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To check the effect of bhagottar gutika and abhyanga in post covid respiratory distress

Clinical Study To Evaluate The Efficacy Of Bhagottar Gutika And Abhyanga In The Management Of Post COVID Respiratory Distress - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056384
Enrollment
40
Registered
2023-08-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: U071- COVID 19 virus identified

Interventions

None listed

Sponsors

Ajit kumar pandey
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age between 18 to 58 years irrespective of sex. 2 Previously confirmed cases of SARS Cov-2 Rt-PCR patients. 3 Post covid Patients presented with symptoms such as SOB, fatigue and insomnia. At least two symptoms must be present out of which one must be SOB. 4 FEV1 greater than 80% of the predicted value. 5 Patients willing to give written consent for participation in the study.

Exclusion criteria

Exclusion criteria: 1 Patients having major systemic illness, renal, hepatic and Autoimmune diseases. 2 Patients who are immunocompromised such as chronic DM and HIV etc. 3 Pregnant and lactating mothers.

Design outcomes

Primary

MeasureTime frame
It is expected that at the end of study we would be able to demonstrate the efficacy of BhagottarGutika & Abhyanga with Amrutaditailam in the management of PCRD.Timepoint: 30 days—

Secondary

MeasureTime frame
this study will helpful in treating respiratory distress patientTimepoint: 15th 30th & 45th day of study—

Countries

India

Contacts

Public ContactAjit Kumar Pandey

Pt Khushilal Sharma Government Autonomous Ayurveda Collage And Institute Bhopal

drvivek.sharma13@gmail.com8770672790

Outcome results

None listed

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