This is a study to know how Vyaghryadi kashayam and bharangi-shunthi churna works in respiratory diseases.

A Randomized Controlled Open Label Clinical Study to Evaluate the Efficacy of Vyaghryadi Kashayam and Bharangi-Shunthi Churna in the Management of Shwasa Roga with special reference to Chronic Obstructive Pulmonary Disease COPD - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/100961

Enrollment

Registered

2026-01-13

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Willing to provide consent Patients who voluntarily agree to participate and provide written informed consent. 2 Patients who fulfill the diagnostic criteria. 3 Patients of age group 40 - 70 years of either gender. 4 Patients who are in a stable phase of COPD ( not experiencing an acute exacerbation in the past 4 weeks). 5 Oxygen saturation (SPO2) more than or equal to 90 percent patients with adequate oxygenation levels without continuous oxygen therapy. 6 Mild to moderate COPD severity- patients with GOLD stage I to II (FEV1 more than or equal to 50 percent predicted but less than 80 percent).

Exclusion criteria

Exclusion criteria: i. Patients not willing to participate in the trial. ii. Patients presenting with complications like advanced Type II respiratory failure, lung collapse, pneumothorax. iii. Patients suffering from other associated major illnesses like malignancy, pulmonary tuberculosis, renal failure, congestive heart failure, ischemic heart disease, severe anemia, myocardial infarction etc. iv. Patients below 40 and above 70 years of age. v. Pregnant and lactating women. vi. Any other condition which the principal investigator thinks may jeopardize the study.

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of Vyaghryadi Kashayam and Bharangi-Shunthi Churna in the Management of Shwasa Roga w.s.r. to Chronic Obstructive Pulmonary Disease (COPD).Timepoint: 30 days	—

Secondary

Measure	Time frame
. To compare the efficacy of Vyaghryadi Kashayam and Bharangi- Shunthi Churna with Doxofylline. ii. To assess the clinical safety of Vyaghryadi Kashayam and Bharangi-Shunthi Churna in the Management of Shwasa Roga w.s.r. to Chronic Obstructive Pulmonary Disease (COPD). Timepoint: 30 days	—

Countries

India

Contacts

Public ContactDr Deeksha Sharma

Rajiv Gandhi Govt Post Graduate Ayurvedic College and Hospital Paprola (HP)

dr.skumarthakur@gmail.com9816195001

Outcome results