Randomized controlled trial2023

Ashwagandha (Withania somnifera) and Shunthi (Zingiber officinale) in mild and moderate COVID-19: An open-label randomized controlled exploratory trial

Singh H, Yadav B, Rai AK, Srivastava S, Saiprasad A, Jameela S, Singhal R, Muralidharan S, Mohan R, Chaudhary S, Rana R, Khanduri S, Sharma BS, Chandrasekhararao B, Srikanth N, Dhiman KS

Complementary therapies in medicine · 8 citations

Review labels

Funding not disclosed

Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.

How it was studied

Design
Randomized controlled trial (indexed by PubMed)
Studied in
People
Main outcome
Health markers and function

Who paid for it

Funding
Funding not disclosed

Publication

Published
2023-07-22 · Complement Ther Med · vol. 76 · p. 102966
Publisher
Elsevier BV
Cited
17 citations · more than 95% of similar papers · 5.3× the field average
Impact
Top 10% most cited in its field
References
53 works
Access
Open access (journal) · CC-BY-NC-ND
Research areas
Phytochemicals and Medicinal Plants · Andrographolide Research and Applications · Piperaceae Chemical and Biological Studies
Keywords
Withania somnifera, Medicine, Zingiber officinale, Adverse effect, Randomized controlled trial, Coronavirus disease 2019 (COVID-19), Traditional medicine, Internal medicine, Clinical trial, Alternative medicine, Disease, Pathology
MeSH
humans, withania, immunoglobulin g, plant extracts, treatment outcome, pandemics, biomarkers, covid-19, zingiber officinale

16 authors

From IN

  • Harbans SinghCentral Council for Research in Ayurvedic Science
  • Babita YadavCentral Council for Research in Ayurvedic Science
  • Amit K. Rai · correspondingCentral Council for Research in Ayurvedic Science
  • Sumit Kumar SrivastavaGovernment Ayurvedic College and Hospital
  • A.J.V. Saiprasad
  • Sophia JameelaCentral Council for Research in Ayurvedic Science

Abstract

Background

Ayurveda interventions have been used for prophylaxis and care during the COVID-19 pandemic in India and have shown promising results in promoting early clinical recovery from COVID-19.

Objective

To assess the efficacy and safety of Ashwagandha [Withania somnifera (L.) Dunal] tablet and Shunthi (Zingiber officinale Roscoe) capsule in mild and moderate COVID-19 compared to conventional standard care.

Methods

A randomized controlled exploratory trial was conducted at a designated COVID-19 care center in India with 60 participants having mild or moderate COVID-19. Ashwagandha, two tablets (250 mg each), and Shunthi, two capsules (500 mg each) twice daily for 15 days, were given orally to the participants in the Ayurveda group (AG) and the control group (CG) received conventional standard care. The outcome measures included clinical recovery rate, the proportion of participants with negative RT-PCR assay for COVID-19 on day 7 and day 15, mean time to attain clinical recovery, change in pro-inflammatory markers, serum IgG for COVID-19, HRCT chest findings, disease progression and incidence of adverse events (AE).

Results

A total of 60 participants were enrolled, and the data of 48 participants (AG = 25 and CG = 23) were considered for the statistical analysis. The mean time for clinical recovery was reduced by almost 50 % in the AG (6.9 days) compared to CG (13.0 days) (p < 0.001). The proportion of participants who attained viral clearance in AG was 76.0 % compared to 60.8 % in the CG (RR= 1.24, 95 % CI: 0.841, 1.851, p-value = 0.270). Changes in the pro-inflammatory markers, serum IgG for COVID-19, and HRCT chest findings were comparable in both groups, and no AE or disease progression was reported.

Conclusions

The Ayurveda interventions, Ashwagandha and Shunthi, can effectively reduce the duration of clinical recovery and improve time for viral clearance in mild and moderate COVID-19. These interventions were observed to be safe and well-tolerated during the duration of the trial.

Trial registration

Clinical Trial Registry of India - CTRI/2020/08/027224.

Abstract via Europe PMC. Copyright remains with the authors or publisher (CC BY-NC-ND).

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