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Efficacy study of Growth Hormone in Chronic Heart Failure

To assess the beneficial effect of adjuvant growth hormone therapy in elderly individuals with chronic congestive heart failure - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068932
Enrollment
150
Registered
2024-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: I504- Combined systolic (congestive) anddiastolic (congestive) heart failure

Interventions

Intervention1: Growth Hormone: To be given in growth hormone deficient chronic heart failure patient Subject will be receive growth hormone in a dose of 0.012 mg/kg every second day (approx. 2.5 IU),

Sponsors

Indian Council Of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Elderly patients, =60and =90 years of age, in outpatient and inpatients, who have 2. Chronic heart failure (with both preserved and reduced ejection fraction) with The New York Heart Association (NYHA) class 2 to 4 irrespective of etiology and whose treatment has not been modified in the past 4 weeks. 3. Patients having growth hormone deficiency 4. Patients are willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Active proliferative or severe non-proliferative diabetic retinopathy, 2.Active malignancy, 3. Any evidence of progression or recurrence of an underlying intracranial tumour 4 Recent myocardial infarction, 5. Severe liver disease, and 6. Serum creatinine levels greater than 2.5 mg/dl.

Design outcomes

Primary

MeasureTime frame
echocardiography in improved ejection fraction (in patients with HFrEF), change in end systolic volume from baseline, LV end diastolic dimension and change in relative wall thickness as a prognostic marker for disease progression Change in functional capacity assessment Blood levels of NT-proBNP Improvement in NYHA classTimepoint: 0,90,180,365 days

Secondary

MeasureTime frame
Change in quality-of-life Change in frailty assessment score Sarcopenia assessment Timepoint: 0,90,180,365 days

Countries

India

Contacts

Public ContactMukesh Kumar

Government Institute of Medical Sciences

saurabhsrivas@gmail.com9654233158

Outcome results

None listed

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