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Study of Shreepad Shree Vallabh SSV Formulation to improve immunity in quarantine patients of COVID-19

An open labelled trial to evaluate safety and efficacy of SSV Formulation to boost immunity in quarantine patients of COVID-19

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024659
Enrollment
30
Registered
2020-04-15
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: B342- Coronavirus infection, unspecified

Interventions

Intervention1: SSV Formulation Tablets: Each tablet of 500 mg to be consumed orally twice a day immediately after meals for 15 days. Control Intervention1: Not Applicable: Not Applicable

Sponsors

SSV Phytopharmaceuticals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Recent history of contact with COVID-19 positive people and are advised to be quarantined or has symptoms which include cough, fever with or without chills and difficulty in breathing. 2. Willing to provide informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence of acute hypoxic respiratory failure. 2. Intensive care unit (ICU) stay. 3. Patients who need mechanical ventilation. 4. Category 6 or 5 based on modified 7-category ordinal scale of clinical status.

Design outcomes

Primary

MeasureTime frame
Improvement in ambulatory patients who are assessed daily for symptoms which include cough, fever with or without chills and difficulty in breathing for the period they are in quarantine. Timepoint: Baseline, telephonically everyday and day 15.

Secondary

MeasureTime frame
The ambulatory patients who did not require artificial ventilation or were not admitted to ICU during the period of quarantine. Improvement in the clinical variables including Pro inflammatory cytokine IL-6 from baseline to end of the quarantine period i.e. 15 days.Timepoint: Baseline, telephonically everyday and day 15. Clinical variables including Pro inflammatory cytokine IL-6 will be recorded at baseline and at day 15.

Countries

India

Contacts

Public ContactDr Samadhan Patil

Shreepad Shree Vallabh SSV Phytopharmaceuticals

yogesh_dound@yahoo.com91-9769057549

Outcome results

None listed

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