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A clinical study TO evaluate the efficacy of AYUSH drug on Covid 19 patients

A clinical study on the efficacy of NF1 AND NF3 IN THE TREATMENT OF COVID 19 POSITIVE PATIENTS ALONG WITH STANDARD CARE

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035908
Enrollment
100
Registered
2021-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

None listed

Sponsors

Sri Sri Institute for advanced research Begaluru Karnataka
Lead Sponsor
Sriveda Sattva Private limited Bangalore Karnataka
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: History of fever Cough Willingness to participate in the study Patient should be ready to give written consent Indian Nationals

Exclusion criteria

Exclusion criteria: Age less than 18 years or more than 65 years Pregnancy and Lactation T2DM CVS disorders Renal Problems(CKD) COPD Bronchial Asthma Malignancy CVA

Design outcomes

Primary

MeasureTime frame
RTPCR NEGATIVE Reducing the signs and symptoms and changes in biomarkersTimepoint: Day5 Day10

Secondary

MeasureTime frame
trial drug will be more effective than placebo change in biomarkersTimepoint: DAY 1 DAY 5 DAY 10

Countries

India

Contacts

Public ContactDr Sanjib Kumar Das

Sri Sri College of Ayurvedic Science and Research Hospital

ayursanjib@gmail.com9437292457

Outcome results

None listed

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