|Year : 2021 | Volume
| Issue : 2 | Page : 256-267
Prospective, randomized, open-label, blinded end point, two-arm, comparative clinical study to evaluate the efficacy and safety of a Fixed Ayurvedic Regimen (FAR) as add-on to conventional treatment in the management of mild and moderate COVID-19 patients
Arun Gupta1, Sasibhushan Vedula1, Ruchi Srivastava1, Sanjay Tamoli2, Narendra Mundhe3, DN Wagh4, Sanjay Batra3, Manoj Patil5, Hiren Baburao Pawar6, Rajiva K Rai1
1 Healthcare Research, Dabur Research and Development Centre, Dabur India Limited, Uttar Pradesh, India
2 Target Institute of Medical Research, Mumbai, India
3 Department of Kayachikitsa, KVTR Ayurveda College and Hospital, Boradi, Shirpur, Maharashtra, India
4 Cottage Hospital, Shripur, Maharashtra, India
5 Covid Care Center, Shingave, Shirpur, Maharashtra, India
6 Sub District Hospital, Shirpur, Dhule, Maharashtra, India
|Date of Submission||25-Mar-2021|
|Date of Decision||12-Apr-2021|
|Date of Acceptance||14-Apr-2021|
|Date of Web Publication||26-May-2021|
Dr. Sasibhushan Vedula
Senior Manager - Healthcare Research, Dabur Research and Development Centre, Dabur India Limited
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: The traditional healthcare systems are being avidly looked into in the quest for effective remedies to tackle the menace of COVID-19 pandemic. Objective: This was a prospective randomized, controlled open-label, blinded end point (PROBE) study to evaluate the efficacy and safety of a fixed ayurvedic regimen (FAR) as an add-on to conventional treatment/standard of care (SOC) in the management of mild-to-moderate COVID-19 infection. Methodology: A total of 68 patients were recruited who consumed either FAR + SOC (n = 35) or SOC only (n = 33) for 28 days. Primary outcomes assessed were mean time required for clinical recovery and proportion of patients showing clinical recovery between the groups. Secondary outcomes assessed included mean time required for testing SARS-CoV-2 negative, change in clinical status on World Health Organization (WHO) ordinal scale, number of days of hospitalization, change in disease progression and requirement of oxygen/intensive care unit admission/ventilator support/rescue medication, health status on WHO quality of life (QOL) BREF, and safety on the basis of occurrence of adverse event/serious adverse event (AE/SAE) and changes in laboratory parameters. Results: Patients consuming FAR as an add-on SOC showed faster clinical recovery from the day of onset of symptoms by 51.34% (P < 0.05) as compared to SOC group. A higher proportion of patients taking FAR recovered within the first 2 weeks compared to those taking only SOC. It was observed that 5 times more patients recovered within 7 days in FAR group when compared to SOC (P < 0.05) group. An earlier clinical recovery was observed in clinical symptoms such as sore throat, cough, loss of taste, and myalgia (P < 0.05). Improvement in postclinical symptoms such as appetite, digestion, stress and anxiety was also observed to be better with the use of FAR. Requirement of rescue medications such as antipyretics, analgesics, and antibiotics was also found to be reduced in the FAR group (P < 0.05). FAR showed a significant improvement in all the assessed domains of QOL. None of the AEs/SAE reported in the study were assessed to be related to the study drugs. Further, FAR did not produce any significant change in the laboratory safety parameters and was assessed to be safe. Conclusion: FAR could be an effective and safe add-on ayurvedic regimen to standard of care in the management of mild and moderate COVID-19 patients. CTRI number: CTRI/2020/09/027914.
Keywords: Chyawanprash, COVID-19, Fixed Ayurvedic Regimen, Giloy, Kalmegh, Tulsi
|How to cite this article:|
Gupta A, Vedula S, Srivastava R, Tamoli S, Mundhe N, Wagh D N, Batra S, Patil M, Pawar HB, Rai RK. Prospective, randomized, open-label, blinded end point, two-arm, comparative clinical study to evaluate the efficacy and safety of a Fixed Ayurvedic Regimen (FAR) as add-on to conventional treatment in the management of mild and moderate COVID-19 patients. J Pharm Bioall Sci 2021;13:256-67
|How to cite this URL:|
Gupta A, Vedula S, Srivastava R, Tamoli S, Mundhe N, Wagh D N, Batra S, Patil M, Pawar HB, Rai RK. Prospective, randomized, open-label, blinded end point, two-arm, comparative clinical study to evaluate the efficacy and safety of a Fixed Ayurvedic Regimen (FAR) as add-on to conventional treatment in the management of mild and moderate COVID-19 patients. J Pharm Bioall Sci [serial online] 2021 [cited 2022 May 24];13:256-67. Available from: https://www.jpbsonline.org/text.asp?2021/13/2/256/316962
| Introduction|| |
COVID-19 has acquired a global pandemic status with increasing morbidity and mortality. Currently, there is no accepted “standard of care (SOC)” available for its management in view of inadequate evidence on existing medicines and their limitations. This is an opportune time when AYUSH concepts and interventions should be evaluated for developing better arsenals to prevent and treat the disease. With this objective, the Ministry of AYUSH has constituted an interdisciplinary AYUSH research and development task force for facilitating research of AYUSH interventions in COVID-19. The current study evaluated the efficacy and safety of a fixed ayurvedic regimen (FAR) of AYUSH interventions – Giloy Ki Ghan Vati, Kalmegh tablets, Tulsi tablets, and Chyawanprash as an add-on to conventional treatment in the management of mild and moderate COVID-19 infection. AYUSH interventions were selected on the basis of traditional wisdom, government recommendation and the abundant published data on their efficacy and safety. Study outcomes were analyzed basis changes in the mean time required for clinical recovery and proportion of patients showing clinical recovery between the groups. This study is one of the earliest clinical trials to evaluate the efficacy and safety AYUSH interventions as add-on to conventional treatment/SOC in COVID-19 patients.
Ethical conduct of the study
The study was approved by the Institutional Ethics Committee of KVTR Ayurved College and Hospital, Boradi, Maharashtra, to be conducted at COVID Care Center, Shingave, Shirpur, Dhule, Maharashtra, and Dedicated COVID Hospital, Cottage Hospital, Shirpur, Dhule, Maharashtra. The study was registered with the Clinical Trial Registry-India (CTRI) on September 19, 2020, vide CTRI number CTRI/2020/09/027914. Study personnel comprised a team of ayurvedic and modern medical doctors trained in good clinical practice for ethical conduction of the study. Study participants gave written informed consent before screening for their participation. An e-consent was also prepared on the lines of written informed consent form. Study data were captured on electronic data capture Electronic Data Capture (EDC) platform.
This was a prospective, randomized, open-label, blinded end point, two-arm, comparative clinical study conducted between September 2020 and January 2021. An independent investigator who was blinded to the group allotted did the assessment of clinical recovery in the study (blind end point assessment). The study data for all the study participants were captured in an electronic case record form (e-CRF) prepared as per 21 CFR compliant, EDC System. All the requirements of standards of safety, quality, and confidentiality of the patients' data were followed for data collection. First patient enrolment was on September 29, 2020. Last patients' last follow-up visit was on January 14, 2021.
Patients were selected from COVID care center/dedicated COVID hospital and comprised male and female patients aged between 18 and 60 years with laboratory-confirmed (reverse transcription-polymerase chain reaction [RT-PCR]/rapid antigen test/any other test for as per the current guidelines) mild-to-moderate SARS-CoV-2 infection of not more than 3 days (≤3 days) as per the MoHFW Government of India (GoI) guidelines [Table 1]., All the included patients expressed their voluntariness to participate in the study and were willing to follow COVID-19 prevention and containment-related guidelines issued from time to time by government/local health authorities throughout the study period.
Patients suffering from severe COVID-19 infection in physician's opinion and fulfilling at least two of the following three criteria: (i) respiratory distress at room ambience (≥30 breaths/min), (ii) oxygen saturation ≤93% at rest on the peripheral digital arterial oximetry and requiring oxygen support for over 1 h to normalize, and (iii) any of the known COVID-19 complications and emergency procedures which may require shift/admission in intensive care unit (ICU) (such as respiratory failure, adult respiratory distress syndrome, and requirement of oxygen support for over 1 h or mechanical ventilation, septic shock, or severe nonrespiratory organ dysfunction or failure) were excluded. Patients having difficulty in swallowing oral medications, chronic, severe, unstable, uncontrolled co-existent medical conditions (diabetes, hypertension, cardiac, liver, kidney, lung disorders, etc.), immune compromised status or any other medical or surgical condition that would require immediate medical or surgical intervention at the time of screening or may put the patient at increased risk during the study, AYUSH system-based contraindications, allergies or known to be allergic to intraperitoneal, pregnancy, lactation or any other condition, which in the opinion of the investigators, would render the patient unsuitable for participation in the study were also excluded.
A sample size of 30 patients in each of the groups was calculated considering the predicted recovery rate and period by the physician and using statistical formula. A 5% level of significance (95% confidence interval) with a statistical power of 80% was considered for calculating sample size. Further, considering the novel COVID-19 pandemic condition and nonavailability of significant amount of epidemiological data to calculate appropriate sample size, a minimum statistically relevant sample size of 60 completers (30 each in the two groups) was considered for the present study.
Study interventions and treatment
Patients in the FAR group were prescribed Giloy Ki Ghan Vati, Tulsi tablets, and Kalmegh tablets – 1 tablet each, two times a day, and 1 teaspoonful (approximately 10–12 g) of Chyawanprash twice daily as add-on to SOC prescribed by concerned health authorities for 28 days.
Giloy Ki Ghan Vati is a classical ayurvedic formulation containing goodness of renowned herb Giloy. Tulsi tablets and Kalmegh tablets are proprietary ayurvedic formulations, containing extracts of Tulsi leaves and Kalmegh roots, respectively, as actives. Chyawanprash is a classical ayurvedic formulation for immunity and overall health containing goodness of over 40 herbs and ingredients. Batch numbers TM00002 Mfd. 8/2020 of Tulsi tablets, BM 6898 Mfd. 09/2020 of Chyawanprash, DRDC/NJT/02 Mfd. 8/2020 of Kalmegh tablets, and SB00142 Mfd. 08/2020 of Giloy Ki Ghan Vati, all manufactured by Dabur India Limited, Ghaziabad, were used in the current study.
Patients in SOC group served as control receiving conventional treatment comprising antibiotics/antiallergics/antipyretics/multivitamins as prescribed/advised by local health authorities for 28 days.
- Mean time (in days) required for clinical recovery from COVID-19 from the day of first noticed symptoms to the day of clinical recovery and from day of randomization to the day of clinical recovery
- Proportion of patients showing clinical recovery between the two groups.
- Mean time (days) required for testing negative for SARS-CoV-2 from the day of randomization and from the day of first noticed symptoms
- Assessment of clinical recovery/postclinical recovery and Ayurvedic clinical assessment
- Number of days of hospitalization
- Change in disease progression and requirement of oxygen/ICU admission/ventilator support/rescue medication
- Change in clinical status on World Health Organization (WHO) ordinal scale and health status on WHO quality of life WHOQOL-BREF
- Global assessment of overall change
- Percent mortality in the groups
- Assessment of safety on the basis of adverse event/serious adverse event (AE/SAEs) and laboratory safety parameters.
| Methodology|| |
At screening visit, a written informed consent was obtained from patients for their participation in the study. Patients' demographic data, medical history, and physical and systemic examinations were done, and vitals and SpO2 levels were recorded. Patients' clinical status was assessed on the 8-point WHO ordinal scale., Patients' laboratory investigations i.e., hematology, blood sugar (Fasting), liver functions, lipid profile, renal functions, HIV status, and urinalysis (routine and microscopic), were done. Chest X-ray and electrocardiogram (ECG) were done if advised by the investigator. For all fertile female patients, a urine pregnancy test was done. Patients fulfilling the inclusion/exclusion criteria were recruited and randomized to either of the study groups as per a computer-generated randomization chart. Both the groups were advised to follow their normal/routine and diet which they were already following. At each visit, patients were enquired for occurrence of any AE/SAE during the period from their last visit. Any AE/SAE was recorded in the CRF. Any other tests such as serum ferritin, serum D-dimer, and CRP, if advised by the health authorities, were done. Patients' ayurvedic clinical assessment was done, and their physical constitution (ayurvedic Dosha Prakriti) and QOL were assessed.
During hospital stay, patients' physical and systemic examinations, vitals, and SpO2 levels were routinely checked. Patients' ayurvedic clinical assessment and clinical status rating on ordinal scale were assessed. Patients were enquired for occurrence of any AE/SAE, and their drug compliance was checked. Assessment of number of patients requiring oxygen, ICU admission and ventilator support, any other higher treatment, or rescue medication was done. Clinical recovery from COVID-19 symptoms was assessed basis criteria mention in [Table 2].
Clinically recovered patients were discharged from the hospital as per hospital guidelines. The mean time (days) required for clinical recovery from the day of randomization and from the day of the first noticed symptom was recorded CRF. Patients' COVID test was repeated at the time of discharge. If it was positive, then the test was to be repeated on day 28. If required, patients' hematological and biochemical parameters or any other tests, if advised, were done, and patients' clinical status and ayurvedic assessment of postclinical recovery (appetite, digestion, sleep, anxiety, physical weakness, etc.) were also done. Number of days of hospital stay was noted in the CRF. Patients were enquired for the occurrence of any AE/SAE during the period from the last visit and their drug compliance was recoded. Discharged patients in both the groups were advised to continue with their respective treatments as advised by the investigators and the local health authorities till day 28 and follow the instructions given by the investigator/local health authorities such as practicing self-isolation, respiratory etiquettes, wearing masks, and physical distancing. The discharged patients were followed up telephonically on day 14 to assess their clinical status and ayurvedic postclinical recovery (appetite, digestion, sleep, anxiety, physical weakness, etc.). Patients were also inquired for the occurrence of any AE/SAE during the period from the last visit and drug compliance.
On day 28 (end of study), patients were called at the study site for final follow-up visit. Their physical and systemic examinations and all clinical assessments were done, and QOL was assessed using the WHO QOL BREF instrument. Patients were enquired for the occurrence of any AE/SAE during the period from the last visit and drug compliance. Patients' global assessment of safety and efficacy was evaluated by the investigator and patients themselves. Patients' laboratory investigations were done. If required, chest X-ray and ECG can be done and serum ferritin, serum D-dimer, and CRP can also be done. RT-PCR/rapid antigen test was repeated for patients who tested positive on discharge from hospital. If patients' report was negative, it was recorded in CRF. In case any patient tested positive on day 28, he was instructed to take further treatment and follow guidelines as prescribed by the local health authorities.
| Observations and Results|| |
A total of 70 patients were screened, out of which there were two screen failures as these patients did not meet the inclusion/exclusion criteria and 68 patients were recruited in the study. Recruited patients were randomized into either of the study groups as per computer-generated randomized list, of which 35 patients were randomized in the FAR/add-on group and 33 patients in the SOC/control group. There were no drop-outs; all the recruited patients completed the study and were considered as completers or efficacy evaluable cases at the end of the study. The study flow is depicted in [Figure 1].
Age- and sex-wise distribution of patients
The average age of the patients was 39.20 ± 11.68 years in the FAR group and 41.06 ± 12.12 years in the control group, showing no significant difference (P > 0.05). Of the 35 patients in FAR group, there were 19 (54.28%) males and 16 (45.72%) females. Of the 33 randomized in the control group, there were 24 (72.72%) males and 9 (27.27%) females. The average body weight and body mass index of the patients at baseline in the FAR and SOC groups was 59.71 ± 9.56 kg and 22.40 ± 2.93 kg/m2 and 62.24 ± 9.414 kg and 22.55 ± 3.238 kg/m2, showing no statistical difference (P > 0.05).
Assessment of Prakriti and Ayurvedic Clinical Parameters
Prakriti wise Analysis
Analysis of Prakriti,,, showed a predominance of Vata-Pitta Prakriti in FAR group. None subjects were of a single Doshic predominance. The SOC group showed a predominance of Pitta-Kapha Prakriti [Table 3]. Ayurvedic clinical assessment done at baseline basis Agni and Kostha, Dosha, Rogibala, Dushya etc,,, showed a predominance of - Vishamagni in FAR Group and Mandagni in SOC group. None of the subjects possessed Tikshnagni. Assessment of Kostha (bowel strength) showed a predominance of Madhyam Kostha in both study groups. Assessment of Rogibala (strength of the patient) showed predominance of Madhyam Bala in both study groups. Maximum subjects in both the groups had Vata predominant conditions (Vata/Vata-Pitta/Vata-Kapha). Subjects in both the study groups showed involvement of Dushya like Rasa, Rakta & Mamsa Dhatu. Assessment of Adhisthan and Strotas revealed maximum involvement of Pranavaha, Annavaha and Rasavaha Srotas (respiratory, digestive and circulatory systems) [Table 4], [Table 5], [Table 6], [Table 7], [Table 8].
Assessment of primary outcomes
Comparative assessment of mean time (days) required for clinical recovery
The average number of days required for clinical recovery from the day of onset of symptoms (1st day of appearance of symptoms) and from the day of randomization in the FAR and SOC groups was 10.77 ± 3.24 and 16.30 ± 5.93 and 8.40 ± 3.10 and 13.73 ± 5.66, respectively. The recovery in the FAR group was assessed to be 51.34% faster from the day of onset of symptoms and 63.45% faster from day of randomization in comparison to the control group [Table 9], [Figure 2] and [Figure 3]. This difference between the groups was found to be statistically significant (P < 0.001), and patients in the FAR group were assessed to have recovered faster and earlier as compared to those in the control group.
|Figure 2: Time to Clinical Recovery (days) from Day of Onset of Symptoms|
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Comparative proportion of patients showing clinical recovery
A higher number of patients (45.71% and 97.14%) taking FAR showed clinical recovery within 1 and 2 weeks (7 and 14 days) from the day of randomization, while in the control group, this number was lesser (9.09% and 69.69%). Statistically, the proportion of patients showing recovery based on the number of days showed a significantly higher number of patients (P < 0.05) achieving earlier clinical recovery in the FAR group as compared to control group. It was observed that 5 times more patients showed clinical recovery in the 1st week in FAR group than control group. All patients recovered completely in both the groups at the end of the study, i.e., 28 days [Figure 4].
|Figure 4: Comparative assessment of proportion of patients showing clinical recovery|
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Assessment of secondary outcomes
Comparative assessment of mean time (days) required for testing negative for SARS-CoV-2
Testing for RT-PCR was done as per the guidelines of the local health authorities for COVID-19. The average number of days required for testing negative for SARS-CoV-2 (on RT-PCR/rapid antigen test) assessed from the day of randomization was 14.74 ± 8.74 and 16.61 ± 10.19 in the FAR and control groups, respectively, while the same was 17.17 ± 8.77 and 19.15 ± 10.46 from the day of onset of symptoms, respectively, in the groups. Although the average number of days for testing negative for SARS-CoV-2 was lesser in FAR group than control group, statistically this difference between the groups was not significant.
Comparative assessment of duration of fever and other clinical symptoms
The common clinical symptoms recorded in the study groups were fever, sore throat, cough, shortness of breath, loss of taste and smell, myalgia, headache, and generalized weakness. The average number of days required for recovery in clinical symptoms was found to be lesser in FAR group as compared to the control group. Patients in FAR group showed a significantly earlier (P < 0.05) recovery in symptoms such as sore throat, loss of taste, myalgia, anorexia, weakness, and vertigo when compared to control [Table 10].
|Table 10: Assessment of number of days for clinical recovery from symptoms of COVID-19|
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Comparative assessment of change in clinical status on World Health Organization ordinal scale
WHO ordinal scale was used to score improvement in clinical status of patients. The total score in FAR group at the time of diagnosis of COVID infection was 105 (n = 35 with a score of 3 each) and 99 (n = 33 with a score of 3 each) in SOC group. During hospitalization, the total score in FAR group was 106 (n = 34 with score of 3 and 1 with score of 4) and 101 in SOC group (n = 31 with score of 3 and 2 patients with score of 4 each). At the end of the study, the score in both the groups was 0 as all the patients recovered.
Comparative assessment of disease progression and requirement of oxygen, intensive care unit admission, ventilator support, and percent mortality
One patient in FAR group and two in control group required oxygen support. One patient required ICU admission in FAR group, while none of the patients required ICU admission in control group. None of the patients required ventilator support in any of the groups. There was no mortality in the study.
Assessment of number of days of hospitalization in the two groups
The average number of days of hospitalization in FAR group was 7.80 ± 2.81 while in the control group was 7.64 ± 3.17. Statistically, there was no significant difference between the groups.
Assessment of postclinical recovery
Post clinical recovery was assessed from baseline to the end of the study basis changes in parameters in parameters such as appetite, digestion, sleep, stress, anxiety, and physical weakness. A higher number of patients in the FAR group showed improvement in their appetite and digestion (74.28% and 54.54%), stress and anxiety levels (71.42% and 54.54%), sleep quality (31.42% and 27.27%), and physical strength levels (80% and 75.75%) in comparison to control group. Comparative assessment between the groups, however, showed no statistical difference.
Comparative assessment of requirement of rescue medications
Patients in both the groups were provided similar SOC consisting of antibiotics, antiallergics, antipyretics, and multivitamins from the day of randomization to discharge. In FAR group, 33 (94.28%) patients were given antibiotics while 32 patients (96.96%) received antibiotics in SOC group during this period. Thirty-one patients (88.57%) required antipyretics/analgesics in FAR group, while the number was 29 (87.87%) in control group. Nineteen patients (54.28%) were given antiallergics/antihistamines in FAR group, while the number was 23 (69.69%) in control group. In FAR group, 31 (88.57%) were advised multivitamins and calcium supplements, while 33 (100%) patients were given these supplements in the control group. Two (5.71%) patients were given steroids in FAR group, while none were given steroid in control group. Further, 2 (5.71%) patients were given antiviral in FAR group, while three patients (9.09%) received antivirals in control group.
From the time of discharge to the end of the study, a statistically higher number of patients in SOC group were found to require rescue medications such as antibiotics and antipyretics/analgesics. None of the patients required steroids after discharge in either of the groups. One patient was given antiviral after discharge in control group, while none required them in FAR group. A total of 11 (31.42%) patients required tonics (multivitamins, calcium supplements) in the FAR group, while 18 (54.54%) required them in the control group [Table 11].
Comparative assessment of changes in quality of life
QOL was assessed using WHO QOL BREF at the baseline, at discharge, and at the end of the study on the basis of changes in four domains, namely physical, psychological, social, and environmental health, as also, the overall QOL and the general health. All the assessed parameters of QOL showed improvement in both the groups at all the evaluated time points. Between the groups analysis, however, showed a significantly better improvement in FAR group in all the domains as compared to control group. There was a 66.11% higher improvement in physical health domain in FAR group as compared to control group [Table 12] and [Figure 5].
|Table 12: Assessment of domain scores on World Health Organization Quality-of-Life Scale BREF Scale|
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|Figure 5: Physical health domain score of World Health Organization-Quality of Life scale|
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Global assessment of overall efficacy and safety as per physician and participants
Global assessment of overall efficacy as per the physician and participants showed improvement in all the patients in both the groups. Majority of the patients taking FAR showed very much improvement both as per investigators and the patients (62.85% and 65.71%), while SOC group showed much improvement (78.78% each). None of the patients in either of the groups showed worsening in the study. Assessment of overall safety by physician showed that maximum patients showed overall safety of FAR followed by good overall safety (71.42% and 25.71%) while assessment as per patients' reported of excellent overall safety of FAR in majority followed by good overall safety (62.85% and 34.28%).
Assessment of safety
Safety evaluation based on occurrence of adverse event/serious adverse event
A total of eight AEs, four in each group, were recorded in the study. The common AEs in the study were loose motions, constipation, retrosternal burning, difficulty in breathing, and joint pains. None of these AEs were assessed to be related to the study products. One SAE was reported in the study in the FAR group which resulted in admission to higher care facility. This SAE, in investigator's opinion, was assessed to be not related to the study products.
Safety evaluation based on laboratory parameters and vitals
Safety evaluation with respect to hematological and biochemical parameters, liver functions, renal functions, lipid profile, and urinalysis done at the baseline and EOS did not show any significant change. Further, no significant change in vital parameters (pulse, temperature, respiratory rate, blood pressure, and SpO2 levels) was observed from baseline to discharge and further till the end of the study in both the study groups.
| Discussion|| |
COVID-19 infection was first reported in Wuhan, China, on December 31, 2019 and has since been recorded in virtually all nations of the world. Since its emergence, the race against time is on globally to assess various existing drugs for COVID-19 and to develop a safe and effective cure for the disease. Many allopathic, herbal, and traditional medicines are being evaluated clinically for their preventive as well as curative roles against SARS-CoV-2. India too has recorded a huge number of cases followed by gradual stability and upsurges in pandemic situation. Many AYUSH drugs including Chyawanprash, Tulsi, and Giloy have been advocated by the GoI for the prevention and management of COVID-19 and are being tested for their beneficial effects in its management., The current study evaluated a FAR of Giloy Ki Ghan Vati, Tulsi tablets, Kalmegh tablets, and Chyawanprash as add-on to conventional treatment/SOC in the management of mild and moderate COVID-19 patients. The rationale for selection of these drugs was traditional wisdom,, and the abundant scientific data on the herbs Giloy (Tinospora Cordifolia Miers), Tulsi (Ocimum sanctum L.) and Kalmegh (Andrographis paniculata (Burm. f.) Nees). A recently concluded clinical study concluded regular consumption of Chyawanprash plays a significant role in the prevention of infections including COVID-19 infection in the current pandemic. The severity of infection-related illnesses including COVID-19 also was found to be lower with the consumption of Chyawanprash. Ministry of AYUSH in its various guidelines has recommended Chyawanprash both as a preventive measure and for aiding post-COVID recovery.,
This study was conducted at dedicated COVID-19 hospital and COVID care center in accordance with guidelines and regulations pertaining to diagnosis, investigations and testing, administration of SOC treatment, and duration of hospital stay in pandemic situation issued by local health authorities. Guidelines issued by the Interdisciplinary Research and Development Task Force, Ministry of AYUSH, GoI, were followed with respect to development of protocol, sample size calculation, CRF development, etc., A total of 68 patients (35 in FAR and 33 in control/SOC group) were recruited in the study all of which completed the study. Primarily, patients of middle-aged males formed the study population. This finding is in line with the global findings where higher incidence of COVID-19 is reported among males compared to females. Assessment of patients on ayurvedic clinical parameters in line with AYUSH guidelines was carried out in this study. Majority of the patients in both groups were found to possess digestive dysfunctions. Predominantly, imbalance of Vata and Kapha Doshas and Rasa and Rakta Dhatus was observed in both the groups. Earlier studies report patients with Vata-Kapha, Pitta-Kapha, and Kapha-dominant Prakriti have been found more affected with COVID-19.
Assessment of Vyadhi Adhisthan (seat of the disease) revealed that Pranvaha, Annavaha, and Rasavaha channels (respiratory, digestive, and circulatory systems) to be predominantly affected in both the groups. The findings are in line with earlier studies on COVID-19 profiling that report involvement of these channels considering febrile condition with respiratory symptoms, such as cough cold and breathing problems. Considering the pathophysiology of infection of novel coronavirus, and the observations of the Ayurvedic assessments of patients in both groups, COVID-19 could be correlated with Bhutabhishangaja Vyadhi/Bhutabhishangaja Jvara which is Samsargaja/Aupasargika in nature (a febrile contagious condition primarily affecting the respiratory system/lungs) described in ayurvedic texts. In earlier researches too, COVID-19 infection had been provisionally understood from the ayurvedic perspective as Vata-Kapha-dominant Sannipatajvara of Agantu origin with Pittanubandha.,
The results of the present study revealed that patients administered FAR as add-on to conventional treatment recovered faster and earlier as compared those administered SOC only, as assessed by the lesser number of days required for clinical recovery from the day of randomization and also from the time of onset of symptoms of COVID-19. The clinical recovery was found to be 63.45% faster in FAR group when compared from the day of randomization and 51.34% faster when compared from the day of onset of symptoms. A significantly higher proportion of patients (P < 0.05) also showed faster and earlier recovery in FAR group as compared to control group within 1 and 2 weeks. No statistically significant difference was observed between the two groups in the mean number of days required for testing negative for SARS-CoV-2 either from the day of randomization or from the day of onset of clinical symptoms.
Only a few patients in both the groups required ICU admission and oxygen support, while none of the patients required ventilator support in the both the groups, possibly due to inclusion of mild-to-moderate COVID infection only. No significant difference was observed in number of days of hospitalization between the groups. All the patients recovered completely toward the end of the study. No mortality was observed in any of the groups. Postrecovery from the illness, FAR group reported a significantly better improvement in appetite and digestion. A significant reduction in stress and anxiety levels was observed in FAR group in comparison to control. Statistically, no difference was observed on physical strength and sleep quality in both the groups. Assessment on WHO QOL parameters showed significantly better improvement in all the QOL parameters in FAR group compared to control group. Global assessment of the overall efficacy as per physician and patients revealed a better improvement in FAR group compared to control group. Assessment basis of requirement of rescue medications (antibiotics, analgesics, antipyretics, antiallergics, etc.) showed a significantly lesser number of patients required these in FAR group in comparison control group. The results of the study establish FAR as an effective add-on to the SOC in the management of mild-to-moderate cases of COVID-19 infection.
Assessment of overall safety as per physician and participants revealed excellent overall safety of both the treatment groups. A total of eight AEs, four in each group, such as loose motion, constipation, and retrosternal burning, were recorded in the study. None of these AEs, however, were assessed to be related to the consumption of the study products. The one SAE recorded in the study in FAR group was also not assessed to be related in investigator's opinion. There was no significant change in the laboratory and vital parameters in both the study groups. These findings validate the safety of FAR as add-on to SOC in the management of mild-to-moderate cases of COVID-19.
The herbs Giloy, Tulsi, and Kalmegh are renowned for their various health benefits in Ayurveda.,, These herbs have exhibited antiviral,,, anti-inflammatory,,, immunomodulatory,,, antiallergic,,, antipyretic,,, and antioxidant,, potential in scientific studies. Chyawanprash is a traditionally renowned ayurvedic health supplement that has been studied extensively in scientific and clinical studies for its immunostimulatory,, antioxidant, and anti-inflammatory potentials. Beneficial effects have also been established on lung health against particulate matter-induced pulmonary disease in mice by estimating various cytokines and immunoglobulin. Chyawanprash has also been established as a prophylactic measure for COVID-19 infection by virtue of its immunity-boosting effects. A better and faster clinical recovery in mild-to-moderate COVID-19 patients administered FAR as an add-on to SOC can be attributed to the synergistic immunity and overall health-boosting effect of the herbs contained in Giloy Ki Ghan Vati, Tulsi tablets, Kalmegh tablets, and Chyawanprash.
Strengths and limitations
FAR as add-on to conventional treatment/SOC resulted in faster and earlier clinical and postclinical recovery in mild-to-moderate-19 infection. A randomized control study with larger sample size and testing of certain laboratory parameters to evaluate the effect on inflammatory biomarkers and cytokines would help in further validation of study results.
| Conclusion|| |
FAR significantly reduced the clinical recovery time in mild-to-moderate COVID-19 infection when used as add-on conventional treatment or the SOC. Patients consuming FAR as an add-on to SOC showed a faster clinical recovery from the day of onset of symptoms by 51.34% (P < 0.05) as compared to SOC group. A significantly higher proportion of patients taking FAR showed recovery within the first 2 weeks as compared to those taking conventional treatment only. It was observed that 5 times more patients recovered within 7 days in FAR group when compared to control. A faster recovery was observed in clinical symptoms such as sore throat, cough, myalgia, and loss of taste. Improvement in postclinical symptoms such as appetite, digestion, stress, and anxiety was observed to be better with the use of FAR. Requirement of rescue medications such as antipyretics, analgesics, and antibiotics was also found to be reduced in FAR group (P < 0.05). Further, FAR showed a significant improvement in all the assessed domains of QOL. None of the AEs/SAEs reported in the study were assessed to be related to study drugs. Further, FAR did not produce any significant change in the laboratory safety parameters and was assessed to be safe.
The study concludes FAR to be an effective and safe ayurvedic regimen as add-on to conventional treatment/SOC in the management of mild and moderate COVID-19 patients. The study outcomes establish the role of AYUSH interventions (FAR) as add-on to conventional treatment in management of newer diseases such as COVID-19 infection.
The authors wish to thank the team involved in the conduct of the study in these challenging times, especially, the team from CRO - Dr Swapnali Mahadik (Senior - Clinical Trial Monitor, Head – EDC, and Data Management), Ms. Mansi Mehta (Senior CRC Mumbai and Clinical Trial Data Manager), Dr. Ruby Dubey (Senior CRC and Data Monitoring Executive), Dr. Shital Raka, Dr. Maya Patil, Dr. Shaligram Nerkar, Dr. Mahendra Shalunke (Clinical Research Coordinators), Dr. Vinay Pawar (Bio-Statistician and Medical Writing), Dr. Vyanketash Shivane (External Medical Expert), Dr. Shikha Mishra, Mr. Karun Wadhwa and Mr. Pankaj Kumar Gupta (Tulsi Tablets & Kalmegh Tablets) & Mr. Dharmendra Kumar (Dabur Chywanprash & Giloy ki Ghanvati) and Dr. Rugvedi Padmanabha (Dabur India Ltd. for Editorial Support).
Financial support and sponsorship
Dabur India Limited.
Conflicts of interest
Arun Gupta, Rajiva K Rai, Sasibhushan Vedula and Ruchi Srivastava are employed with Dabur India Limited.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7], [Table 8], [Table 9], [Table 10], [Table 11], [Table 12]