Skip to content

A clinical trial to study the effect of standard treatment of heart failure on plasma levels of Apelin in patients with heart failure.

Effect of Therapy on Plasma Apelin Levels in Patients of Heart Failure.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2009/091/000935
Enrollment
50
Registered
2010-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Heart Failure, Apelin

Interventions

Intervention1: PTMC: Non pharmacoogical Intervention2: Standard drugs: Diuretics, ACE inhibitors, beta-blockers in standard doses Control Intervention1: NIL:

Sponsors

Department of Pharmacology AIIMSAnsari NagarNew Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult male or female patients aged between 12 and 80 years Systolic or diastolic heart failure of NYHA class II or more Mitral stenosis patients posted for Percutaneous Transluminal Mitral Commissurotomy (PTMC) Healthy age matched controls with normal cardiovascular function

Exclusion criteria

Exclusion criteria: Diabetes mellitus Obesity Hypercholesterolemia Severe or uncontrolled hypertension Hepatic or renal failure Pregnant or lactating women (except for PTMC group) History of any acute coronary syndrome within previous one month

Design outcomes

Primary

MeasureTime frame
Change in plasma apelin levels with therapy over a follow up period of 12 weeks.Timepoint: Baseline, 1 hour, 14-18 hours and at 12 weeks after PTMC in mitral stenosis patients undergoing the surgery. At baseline and after 12 weeks in other study groups, namely systolic heart failure, diastolic heart failure and healthy control groups.

Secondary

MeasureTime frame
-Plasma apelin levels in heart failure patients compared to normal controls at baseline. -Correlation between plasma apelin levels and plasma BNP levels, echocardiographic variables and quality of life parameters over a follow up period of 12 weeks. Timepoint: Baseline and at 12 weeks.

Countries

India

Contacts

Public ContactDr Vinu Wilson

A.I.I.M.S.

vinuwilson85@gmail.com01126593540

Outcome results

None listed

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