Clinical Trials Directory

Trials / Completed

CompletedNCT00841139

Metabolic Manipulation in Chronic Heart Failure

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
50 (actual)
Sponsor
University Hospital Birmingham NHS Foundation Trust · Academic / Other
Sex
All
Age
16 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Conventional measures used for the treatment of chronic heart failure act predominantly by reducing the work performed by the heart. In a recent study, the investigators showed that one drug (perhexiline) substantially improved symptoms and cardiac function in heart failure. The investigators wish to confirm these findings and test whether or not this drug acts by altering the heart's energy source thus augmenting the energetic status and work efficiency of the heart.

Detailed description

Perhexiline maleate is an antianginal agent which increases the efficiency of energy production by shifting substrate utilisation from free fatty acids towards glucose. We showed that perhexiline therapy was highly effective in improving exercise capacity, symptoms and cardiac function in patients with systolic heart failure of both ischaemic and non ischaemic aetiology. Perhexiline acts by inhibiting both carnitine palmitoyl transferase-1 (CPT-1) and CPT-2, which are key enzymes in mitochondrial free fatty acid uptake. This leads to increased myocardial glucose substrate utilization. Further we wish to ascertain whether or not this drug improves cardiac energetics and efficiency by altering substrate utilization. In this proposal we will assess the cardiac function (by cardiac Magnetic Resonance Imaging MRI), cardiac energetic status (by cardiac Magnetic Resonance Spectroscopy MRS), cardiac efficiency (via pressure-volume loops) and substrate utilization (via left and right heart catheterization), following one month of perhexiline therapy or placebo in patients with symptomatic idiopathic dilated cardiomyopathy on optimal conventional heart failure medications. An interim analysis is planned after 20 patients.

Conditions

Interventions

TypeNameDescription
DRUGPerhexiline100mg o bd
DRUGPlacebo1 tablet bd

Timeline

Start date
2009-02-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2009-02-11
Last updated
2011-11-29

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00841139. Inclusion in this directory is not an endorsement.