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Study to analyse the effectiveness of Yoga in patients with Pulmonary hypertension

Yoga in Pulmonary hypertension: Open label, multi centric, randomized controlled clinical trial - NIL

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092212
Enrollment
246
Registered
2025-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: I272- Other secondary pulmonary hypertension Health Condition 2: I278- Other specified pulmonary heart diseases Health Condition 3: I270- Primary pulmonary hypertension

Interventions

Intervention1: Yoga based cardiac rehabilitation programme (Yoga-CaRe): Yoga based cardiac rehabilitation programme comprising of yogic practices such as asana, pranayama meditation and lifestyle prac

Sponsors

Central Council for Research in Yoga and Naturopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with pulmonary hypertension, defined as peak tricuspid regurgitation velocity of more than 3.5meters per second by 2 dimensional echocardiogram. Stable on medications for 3 months prior to enrollment WHO functional class II and III 6MWD less than 440m

Exclusion criteria

Exclusion criteria: Patients who choose to get recruited in the cardiopulmonary rehabilitation program. WHO functional class 1 and 4. Recent episode of syncope within less than 1 month. Recent acute coronary event within less than 3 months Evidence of left heart failure. Pregnant or planning to get pregnant in the study period. Uncontrolled arrhythmia. Unstable angina. Practicing yoga regularly more or enrolled in cardiac rehabilitation program. Participating in any other clinical trial Significant neuromuscular complications inhibiting participation in the trial. Significant hepatic or renal dysfunction Enzymes more than 2 times normal or Serum creatinine more than 2 times.

Design outcomes

Primary

MeasureTime frame
The six-minute walk distance obtained from the six-minute walk testTimepoint: At baseline, three months and six months

Secondary

MeasureTime frame
WHO functional classTimepoint: Baseline, three months and six months;Quality of life assessment using emPHasis 10 questionnaireTimepoint: baseline, three months and six months;Cardiopulmonary exercise testTimepoint: Baseline and six months;EchocardiogramTimepoint: At baseline, three months and six months;N terminal pro brain natriuretic peptideTimepoint: Baseline and six months;Interleukin 6Timepoint: At baseline and six months;high sensitivity CRPTimepoint: At baseline and six months;Heartrate variabilityTimepoint: At baseline and six months

Countries

India

Contacts

Public ContactDr Ambalam M Chandrasekaran

Centre for Chronic Disease Control, Department of Clinical Trials,

chandrasekaran@ccdcindia.org01141618456

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026