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临床试验/NCT00113698
NCT00113698终止3 期

Trial of ACE Inhibition in Children With Mitral Regurgitation After Repair of AVSD

University of Utah7 个研究点 分布在 2 个国家目标入组 5 人开始时间: 2004年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
5
试验地点
7
主要终点
Comparison of the effect of ACE-I therapy with that of placebo on left ventricular size

研究概览

简要总结

This study will evaluate the efficacy and safety of angiotensin converting enzyme inhibition (ACE-I) therapy for the treatment of mitral regurgitation (MR).

详细描述

BACKGROUND:

MR causes volume overload and hemodynamic burden on the left ventricle. Initial compensatory mechanisms may fail, leading to increased severity. Patients who have had repair of an atrioventricular septal defect (AVSD) are selected for this study as they have a relatively high incidence of moderate MR and their regurgitant orifice is mobile and dynamic, contributing to the likelihood that they might respond to medical therapy.

DESIGN NARRATIVE:

This is a randomized, double-blind, placebo-controlled trial of ACE-I therapy in children less than 18 years of age with at least moderate MR who are at least 6 months postoperative from repair of an AVSD. A non-randomized Observational Phase enrolled 181 children who were less than 6 months postoperative from repair of an AVSD, who were then evaluated at 6 months for trial eligibility.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Children less than 18 years of age and at least 6 months post AVSD repair or reoperation
  • At least moderate MR
  • Asymptomatic or minimally symptomatic, defined by Ross Heart Failure Class I or II
  • Atrioventricular synchrony (paced or intrinsic)

排除标准

  • Tetrology of Fallot, total or partial anomalous venous connection
  • More than trivial MS or outflow obstruction
  • Other sources of LV volume overload
  • Hypertrophic obstructive cardiomyopathy
  • Significant residual coarctation

研究组 & 干预措施

1

Placebo Comparator

干预措施: Placebo (Other)

2

Active Comparator

Ace inhibition (enalapril)

干预措施: Enalapril (Drug)

结局指标

主要结局

Comparison of the effect of ACE-I therapy with that of placebo on left ventricular size

时间窗: Measured after six months of therapy

次要结局

  • Comparison of the effect of ACE-I therapy with placebo on MR severity, left ventricular geometry, hemodynamics, and signs and symptoms of congestive heart failure(6 months on study drug)
  • Evaluation of the early natural history of MR in the six months after repair of an AVSD(6 months on study drug)
  • Comparison of the incidence of adverse events occurring in subjects treated with ACE-I therapy to that in subjects receiving placebo (measured after six months of therapy)(6 months on safety drug)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lois LuAnn Minich

Primary Investigator

University of Utah

研究点 (7)

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