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Effect of AYUSH 64 in COVID 19

Efficacy of Ayurveda Intervention (AYUSH 64) as add-on therapy in COVID 19 patients - An open label randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025855
Enrollment
200
Registered
2020-06-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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: AYUSH 64: AYUSH 64 02 Capsules of 500mg each orally thrice daily for 14 days as add-on therapy to supportive and symptomatic allopathic treatment for COVID 19 patients Control Intervent

Sponsors

IPGT and RA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Asymptomatic or minimal symptomatic COVID 19 patients Patients having 0 to 4 score as per the WHO ordinal scale for clinical improvement Age 18 to 70years Patients who can take oral medicine Patients who are ready to give written consent

Exclusion criteria

Exclusion criteria: Age below 18 and above 70years Patients having severe symptoms of COVID19 Patients on mechanical ventilator or organ support Patients do not able to take oral medication Pregnant and lactating women Oncological diseases and other systemic uncontrol conditions such as HTN diabetes etc Liver or kidney malfunctions. Severe pneumonia Acute respiratory distress syndrome Sepsis and Septic Shock

Design outcomes

Primary

MeasureTime frame
Ordinal scale for Clinical improvement as per WHO Duration on mechanical ventilator All cause mortality Timepoint: 0 7 14 and 28th day

Secondary

MeasureTime frame
Number of patients developed symptomsTimepoint: 0 14 and 28th day;Number of patients who needed oxygen therapyTimepoint: 0 14 and 28th day;Number of patients who needed mechanical ventilatorTimepoint: 0 14 and 28th day;Total duration of symptomatic phaseTimepoint: 0 14 and 28th day;Duration on oxygen therapyTimepoint: 0 7 14 and 28th day;Number of cases reporting any ADR AE Timepoint: 0 7 14 and 28th day

Countries

India

Contacts

Public ContactDr Sagar M Bhinde

IPGTRA Jamnagar

kaurmandip22@yahoo.com9427572306

Outcome results

None listed

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