Ashwagandha Extract Safe Over 24 Weeks in 1,200-Adult Trial
A multicentre trial on 1,200 vaccinated adults found standardised Ashwagandha root extract well tolerated for 24 weeks with no liver or kidney injury.

Why in News
The Ministry of Ayush highlighted a multicentre clinical trial, published in Frontiers in Medicine, which found standardised Ashwagandha root extract safe and well tolerated over 24 weeks in 1,200 vaccinated adults.
A large clinical study on standardised Ashwagandha root extract has reported that taking it every day for 24 weeks was well tolerated and left no sign of injury to the liver or the kidneys. The paper appeared in the journal Frontiers in Medicine on 20 August 2026, and the Ministry of Ayush has drawn attention to what it means for evidence-based Ayurveda.
How the trial was designed
It was a randomised, double-blind, placebo-controlled trial run at seven sites in India. A total of 1,200 apparently healthy adults between 18 and 70 years of age took part, all of whom had received a first, second or booster dose of the COVISHIELD vaccine. Each participant was assigned either a daily dose of 500 mg of a standardised aqueous root extract, equal to 4 grams of raw root powder, or a matching placebo. The trial carries the registration number of the Clinical Trials Registry-India.
Who ran it
Forty-five researchers from nine institutions worked on the study, drawing on Ayurveda, clinical medicine, rheumatology and integrative health. The institutions include the Central Council for Research in Ayurvedic Sciences (CCRAS), the All India Institute of Ayurveda, the National Institute of Ayurveda at Jaipur, the Translational Health Science and Technology Institute and Savitribai Phule Pune University. Dr Arvind Chopra of the Centre for Rheumatic Diseases, Pune, was the lead author.
What the results showed
Participants took the intervention for 24 weeks and were followed to week 28. Of the 1,200 enrolled, 1,032, or 86 per cent, finished the study. Liver enzymes, bilirubin, creatinine and blood urea all stayed within the reported reference ranges. No serious adverse event was traced to the intervention and nobody dropped out because of one. The extract also left the vaccine response alone: virus-neutralising activity was above 85 per cent in both the extract and placebo arms, with no statistically significant gap between them.
What officials said
Ayush Secretary Vaidya Rajesh Kotecha said high-quality clinical research strengthens the scientific base of Ayurveda and supports its responsible use worldwide. Prof. Bhushan Patwardhan, National Professor of Ayush and a co-author, called the work an example of evaluating Ayurveda through modern trials without losing its traditional grounding. Prof. Rabinarayan Acharya, Director General of CCRAS, said such well-designed studies matter for the evidence-informed use of standardised Ayurvedic preparations.
Important Facts
| Intervention | Standardised aqueous Ashwagandha root extract, 500 mg daily |
|---|---|
| Equivalent to | 4 grams of raw root powder |
| Duration | 24 weeks, with follow-up to week 28 |
| Participants | 1,200 healthy adults aged 18 to 70, all COVISHIELD vaccinated |
| Completed | 1,032 participants, or 86 per cent |
| Study sites | Seven in India |
| Researchers | 45 researchers from nine institutions |
| Lead author | Dr Arvind Chopra, Centre for Rheumatic Diseases, Pune |
| Journal | Frontiers in Medicine, published 20 August 2026 |
| Ayush Secretary | Vaidya Rajesh Kotecha |
| CCRAS Director General | Prof. Rabinarayan Acharya |
Exam Point of View
Remember the duration of 24 weeks, the sample of 1,200 adults aged 18 to 70, the daily dose of 500 mg equal to 4 grams of raw root powder, the completion figure of 1,032 or 86 per cent, the journal Frontiers in Medicine, the lead author and CCRAS as the nodal research council.
Practice Questions
How many participants were enrolled in the multicentre clinical trial on standardised Ashwagandha root extract?
- A.600
- B.900
- C.1,200
- D.1,500
Show answer
The randomised, double-blind, placebo-controlled trial enrolled that many apparently healthy adults between eighteen and seventy years of age, each of whom had already received a first, second or booster dose of the COVISHIELD vaccine, across seven study sites in India.
Read the full explanation →What daily dose of standardised aqueous Ashwagandha root extract was given to participants in the trial?
- A.250 mg
- B.500 mg
- C.750 mg
- D.1,000 mg
Show answer
Participants were randomly assigned to receive either this standardised aqueous extract or a matching placebo, and the assignment was double-blind, meaning neither the participants nor the assessors knew which arm a person belonged to.
Read the full explanation →The Ashwagandha safety study was published in which journal?
- A.The Lancet
- B.Frontiers in Medicine
- C.Nature Medicine
- D.Indian Journal of Medical Research
Show answer
The Lancet is wrong because the study was not carried in it, although it is among the best known medical journals and therefore a tempting distractor.
Read the full explanation →Frequently Asked Questions
What did the Ashwagandha trial find?
Daily use of standardised Ashwagandha root extract for 24 weeks was well tolerated, with liver and kidney parameters within reference ranges and no treatment-related hepatic or renal injury.
How many people took part in the trial?
1,200 apparently healthy adults aged 18 to 70 were enrolled across seven study sites in India, and 1,032 of them, or 86 per cent, completed the study.
Did Ashwagandha affect vaccine-induced immunity?
No. Virus-neutralising activity exceeded 85 per cent in both the Ashwagandha and placebo groups, with no statistically significant difference between them.
Which body led the research?
The Central Council for Research in Ayurvedic Sciences was among nine institutions involved, with 45 researchers in all. Dr Arvind Chopra of Pune was the lead author.
Sources
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