Kabasura Kudineer (KSK), a poly-herbal Siddha medicine, reduced SARS-CoV-2 viral load in asymptomatic COVID-19 individuals as compared to vitamin C and zinc supplementation: findings from a prospective, exploratory, open-labeled, comparative, randomized controlled trial, Tamil Nadu, India.
- 2021-09-15
- Trials 22(1)
- S Natarajan
- C Anbarasi
- P Sathiyarajeswaran
- P Manickam
- S Geetha
- R Kathiravan
- P Prathiba
- M Pitchiahkumar
- P Parthiban
- K Kanakavalli
- P Balaji
- PubMed: 34526104
- DOI: 10.1186/s13063-021-05583-0
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Population
- asymptomatic COVID-19 patients aged 18-55 without comorbidities
- Methods
- Prospective, single-center, open-labeled, randomized controlled trial; KSK 60 mL twice daily for 7 days vs standard of care (vitamin C 60,000 IU and zinc 100 mg daily for 7 days)
- Blinding
- Open-label
- Duration
- 7 days
Introduction
Despite several ongoing efforts in biomedicine and traditional medicine, there are no drugs or vaccines for coronavirus disease 2019 (COVID-19) as of May 2020; Kabasura Kudineer (KSK), a polyherbal formulation from India's Siddha system of medicine, has been traditionally used for clinical presentations similar to that of COVID-19. We explored the efficacy of KSK in reducing viral load and preventing the disease progression in asymptomatic, COVID-19 cases.Methods
A prospective, single-center, open-labeled, randomized, controlled trial was conducted in a COVID Care Centre in Chennai, India. We recruited reverse-transcription polymerase chain reaction (RT-PCR)-confirmed COVID-19 of 18 to 55 years of age, without clinical symptoms and co-morbidities. They were randomized (1:1 ratio) to KSK (60 mL twice daily for 7 days) or standard of care (7 days supplementation of vitamin C 60,000 IU morning daily and zinc 100 mg evening daily) groups. The primary outcomes were reduction in the SARS-CoV-2 load [as measured by cyclic threshold (CT) value of RT-PCR], prevention of progression of asymptomatic to symptomatic state, and changes in the immunity markers including interleukins (IL-6, IL-10, IL-2), interferon gamma (IFNγ), and tumor necrosis factor (TNF α). Siddha clinical assessment and the occurrence of adverse effects were documented as secondary outcomes. Paired t-test was used in statistical analysis.Results
Viral load in terms of the CT value (RdRp: 95% CI = 1.89 to 5.74) declined significantly on the seventh day in the KSK group and that of the control group, more pronounced in the study group. None progressed to the symptomatic state. There was no significant difference in the biochemical parameters. We did not observe any changes in the Siddha-based clinical examination and adverse events in both groups.Conclusion
KSK significantly reduced SARS-CoV-2 viral load among asymptomatic COVID-19 cases and did not record any adverse effect, indicating the use of KSK in the strategy against COVID-19. Larger, multi-centric trials can strengthen the current findings.Trial registration
Clinical Trial Registry of India CTRI2020/05/025215 . Registered on 16 May 2020.Research Insights
None progressed to the symptomatic state.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
Viral load in terms of the CT value ... declined significantly on the seventh day in the KSK group and that of the control group, more pronounced in the study group.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
None progressed to the symptomatic state.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
There was no significant difference in the biochemical parameters.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
Viral load in terms of the CT value ... declined significantly on the seventh day in the KSK group and that of the control group, more pronounced in the study group.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg evening daily for 7 days
Adverse Events Reported
We did not observe any changes in the Siddha-based clinical examination and adverse events in both groups.
- Finding
- Reported
We did not observe any changes in the Siddha-based clinical examination and adverse events in both groups.
- Finding
- Reported