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A clinical trial to study the effect of two drugs, Uraria rufescens and Prishnaparni (Uraria picta)in patients suffering from cough (Kasa).

Pharmacotherapeutic evaluation of Uraria rufescens (DC.) Schindl panchanga as an alternative to Prishnaparni (Uraria picta. Desv) panchanga in Kasahara Karma. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088170
Enrollment
100
Registered
2025-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: R05- Cough

Interventions

None listed

Sponsors

Institute of Teaching and Research in Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having classical signs and symptoms of Vataja, Pittaja and Kaphaja Kasa as per diagnostic criteria. 2. Age group: 18-60 years. 3. Chronicity less than 1 month. 4. Newly diagnosed cases of Kasa. 5. Uncomplicated cases of Kasa

Exclusion criteria

Exclusion criteria: 1. Patients suffering from any known systemic disorders (like Tuberculosis, Asthma, etc.) and having Kasa as a complication of any disease will be excluded from the study. 2. Asadhya or Yapya Kasa like Kshayaja and Kshataja. 3. Other known complicated respiratory diseases have organic lesions such as tumors or any anatomical defect in the airway. 4. Uncontrolled systemic disorders like Hypertension, Diabetes Mellitus. 5. Pregnant women and lactating mothers.

Design outcomes

Primary

MeasureTime frame
Changes in scoring patterns developed for grading the clinical factors of Kasa on the 0th, 7th & 14th days.Timepoint: 14th day

Secondary

MeasureTime frame
1. Number of Adverse Events 2. Changes in CBC, SGPT & Serum Creatinine Timepoint: 0th day and 14th day.

Countries

India

Contacts

Public ContactMeghna

Institute of Teaching and Research in Ayurveda,Jamnagar, Gujarat.

brpayu@itra.edu.in7487876343

Outcome results

None listed

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