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临床试验/NCT00154050
NCT00154050已完成不适用

High Dose Candesartan Versus Quinapril for Restenosis Prophylaxis After Stent Angioplasty

Technische Universität Dresden2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2004年5月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
22
试验地点
2
主要终点
Restenosis/reintervention after 6 months

研究概览

简要总结

The study is designed to test the hypothesis that high dose candesartan treatment compared to quinapril is able to reduce intima hyperproliferation and the restenosis rate after stent angioplasty in peripheral occlusive artery disease.

详细描述

Patients are randomly assigned to treatment with either candesartan 32 mg/d or Quinapril 20 mg/d before the angioplasty. Walking distance, intima media thickness and crurobrachial pressure ratios are compared after 6 weeks, 3 months and 6 months. After 6 months an angiographic control is performed.

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • male and female
  • peripheral occlusive arterial disease Stad IIb Fontaine classification

排除标准

  • patients with lesions not available for PTA
  • renal insufficiency
  • patients on calcium-antagonists

结局指标

主要结局

Restenosis/reintervention after 6 months

次要结局

  • crurobrachial pressure ratios
  • pain-free walking distance

研究者

申办方类型
Other

研究点 (2)

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