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临床试验/NCT00841139
NCT00841139已完成2 期

Metabolic Manipulation in Chronic Heart Failure

University Hospital Birmingham NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2009年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50
试验地点
2
主要终点
Change in cardiac energetics as demonstrated by resting myocardial PCr/ATP ratio from cardiac MRS

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
16 Years 至 90 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Optimally-medicated idiopathic dilated cardiomyopathy
  • Symptomatic ( NYHA IIb-III)
  • Impaired left ventricular systolic function (EF < 40%)

排除标准

  • Abnormal liver function tests (defined as above twice the upper limit of normal (ULN))
  • Concomitant use of Amiodarone , Quinidine , Haloperidol or Selective serotonin (5HT) uptake inhibitors such as Fluoxetine and Paroxetine which may inhibit the CYP2D6 enzyme.
  • Pre-existing evidence of peripheral neuropathy.
  • Women of childbearing potential.
  • Patients with implantable cardiac devices (or any other contraindication to MRI).
  • Obesity ( BMI > 32)
  • Obstructive sleep apnea syndrome
  • Patients with known hypersensitivity to perhexiline
  • Patients with impaired renal function (Creatinine > 250 µmol/L)
  • Valvular heart disease defined as more than moderate valvular stenosis or regurgitation.
  • Atrial Fibrillation

研究组 & 干预措施

Perhexiline

Experimental

perhexiline 100mg bd for 1 month duration

干预措施: Perhexiline (Drug)

Placebo

Placebo Comparator

placebo one tablet bd for 1 month duration

干预措施: Placebo (Drug)

结局指标

主要结局

Change in cardiac energetics as demonstrated by resting myocardial PCr/ATP ratio from cardiac MRS

时间窗: 1 Month

次要结局

  • Change in mechanical efficiency (external work / MVO2)(1 Month)
  • Change in respiratory quotient(1 Month)

研究者

发起方
University Hospital Birmingham NHS Foundation Trust
申办方类型
Other
责任方
Principal Investigator
主要研究者

Roger Beadle

Research Fellow to Professor MP Frenneaux

University Hospital Birmingham NHS Foundation Trust

研究点 (2)

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