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Clinical trial of ShatPlus in SARS-CoV-2 Infection.

Clinical trial to evaluate the safety and efficacy of ShatPlus an Ayurvedic Proprietary Medicine as an intervention in adult patients with SARS-CoV-2 infection.

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025340
Enrollment
60
Registered
2020-05-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere

Interventions

Intervention1: ShatPlus along with standard treatment: 10 ml thrice a day ShatPlus along with standard treatment Control Intervention1: Standard treatment: Standard treatment as per protocol of ICMR

Sponsors

BVG Life Sciences Ltd BVG Group
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: SARS-CoV-2 positive nasopharyngeal swab Mild to Moderately severe disease (NEWS score Signed informed consent must be obtained and documented according to AYUSH GCP, and national/local regulations

Exclusion criteria

Exclusion criteria: Requiring ICU admission at screening History of MI, Epileptic episodes Any other comorbidity which is at critical stage at screening Any other condition by which subject proves unfit from investigator perspective

Design outcomes

Primary

MeasureTime frame
No. of days for negative PCR confirmatory test from nasopharyngeal swab for SARS-Covid 2 Serum levels of CD4, CD8, NK cell panel CD16/CD56, CRP, IgM, IgGTimepoint: From baseline to end of study ie 10 days

Secondary

MeasureTime frame
Clinical status of severity Change in National Early Warning Score Hematological parameters like WBS, RBC and platelet count etc. Change in clinical symptom presentation No. of days for negative PCR confirmatory test for SARS-Covid 2 Requirement of admission to intensive care unit Duration of hospital admission Total days admitted to the hospitalTimepoint: From baseline to end of study ie 10 days

Countries

India

Contacts

Public ContactDr Pawan Kumar Singh

BVG Life Sciences Ltd. (BVG Group)

pawan.singh@bvglife.com9409616256

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026