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| ID | Type | Description | Link |
|---|---|---|---|
| RRK 3147 | Other Identifier | Research and Development | |
| MREC 08/H1207/84 | Other Identifier | Ethics | |
| EudraCT 2006-001109-28 | Registry Identifier | European Clinical Trials |
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Up to half of all patients with clinical features of heart failure are found to have normal heart pumping function. Recently the investigators have shown that a drug called perhexiline markedly improved exercise capacity and symptoms in patients with heart failure associated with impaired cardiac pump function. In this proposal the investigators will assess whether perhexiline has beneficial effects in patients with heart failure and a normal heart pumping function.
Up to 50% of patients with symptoms of heart failure have a preserved left ventricular ejection fraction (HFpEF syndrome). Current therapy for systolic heart failure is targeted at inducing vasodilation and counteracting neuro-endocrine activation. There is a lack of a corresponding evidence base for the treatment of HEpEF. We have previously shown that perhexiline, an agent that increases the efficiency of energy production by shifting substrate utilization from free fatty acids towards glucose, was highly effective in improving exercise capacity, symptoms and cardiac function in patients with systolic heart failure. We have also recently shown that energy deficiency plays a major role in the pathophysiology of HFpEF. In this proposal we therefore aim to investigate the effectiveness of perhexiline in 70 HFpEF patients, in a 3 month randomised, double-blind, controlled trial. An interim analysis is planned after 20 patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Perhexiline | Experimental | perhexiline 100mg o bd for 3 months |
|
| Placebo | Placebo Comparator | Placebo one tablet bd for 3 months |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Perhexiline | Drug | 100mg o bd for 3 months |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Peak oxygen consumption (Vo2max) | 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Symptomatic Status (Modified Minnesota Living with Heart Failure Questionnaire) | 3 Months | |
| Resting myocardial energetics by cardiac MR spectroscopy (MRS) | 3 months | |
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Inclusion Criteria:
HFpEF will be defined as:
Patients recruited will be in sinus rhythm
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Michael P Frenneaux, MBBS MD | University of Aberdeen | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Aberdeen | Aberdeen | AB25 2ZD | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25495811 | Derived | Singh S, Beadle R, Cameron D, Rudd A, Bruce M, Jagpal B, Schwarz K, Brindley G, Mckiddie F, Lang C, Dawson D, Frenneaux M. Randomized double-blind placebo-controlled trial of perhexiline in heart failure with preserved ejection fraction syndrome. Future Cardiol. 2014 Nov;10(6):693-8. doi: 10.2217/fca.14.62. |
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| ID | Term |
|---|---|
| D054144 | Heart Failure, Diastolic |
| ID | Term |
|---|---|
| D006333 | Heart Failure |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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| ID | Term |
|---|---|
| D010480 | Perhexiline |
| ID | Term |
|---|---|
| D010880 | Piperidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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| Placebo | Drug | Placebo one tablet bd for 3 months |
|
|
| Resting and exercise diastolic function (nuclear studies) |
| 3 months |
| Indirect measures of resting LVEDP (tissue Doppler E/Ea) | 3 months |
| Global LV Ejection Fraction (MRI / nuclear studies) | 3 months |