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临床试验/NCT00480051
NCT00480051已完成3 期

RESynchronisation in Patients With Heart Failure and a Normal QRS Duration

Heart of England NHS Trust4 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2007年7月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
60
试验地点
4
主要终点
Improvements in 6-min walking distance

研究概览

简要总结

Patients who have heart failure and have electrical evidence of delay in the contraction of the left ventricle on an ECG tracing of the heart are eligible for biventricular pacing. Recent work has suggested that patients with heart failure who do not have electrical evidence of conduction delay (normal QRS) may benefit from biventricular pacing. The reliance on ECGs to determine the presence of dyssynchrony is widespread, although the ECG alone is not 100% sensitive and specific. ECG criteria for de-synchrony in heart failure patients are estimated to pick up only 30% of patients with dyssynchrony, and results in patients missing out on a potentially important treatment advance.

We would like to study patients with heart failure who have normal ventricular activation on their ECGs to see whether we can predict those patients who will respond to biventricular pacing.

详细描述

AIMS and Objectives A randomised controlled clinical trial

Primary objective

• Improvements in 6-min walking distance

Secondary objectives Determine

  1. Symptomatic improvement in quality of life, using the Minnesota Living with Heart Failure questionnaire
  2. Change in NT pro-BNP and echocardiographic parameters of LV function
  3. Does MRI Dyssynchrony Index (CMR-TSI) predicts responders.
  4. Morbidity and Mortality using CARE-HF definitions
  5. Packer combined clinical composite score

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
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Sinus rhythm
  • Symptomatic heart failure - NYHA class III or IV
  • ECG QRS duration less than 120 milliseconds
  • LV ejection fraction of less than 35% on echo
  • Able to give informed consent

排除标准

  • Age below 18
  • Current or planned pregnancy
  • Patient refusal
  • Ventricular tachycardia or ventricular fibrillation
  • Current or recent (within last 30 days) involvement in other studies
  • Requires implantable cardioverter defibrillator (ICD)

结局指标

主要结局

Improvements in 6-min walking distance

时间窗: 6 months

次要结局

  • Symptomatic improvement in quality of life, using the Minnesota Living with Heart Failure questionnaire(6 months)
  • Does MRI Dyssynchrony Index (CMR-TSI) predicts responders(6 months)
  • Change in NT pro-BNP and echocardiographic parameters of LV function(6 months)

研究者

发起方
Heart of England NHS Trust
申办方类型
Other
责任方
Sponsor

研究点 (4)

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