NCT00855673已完成4 期
Intermittent Mechanical Compression For Peripheral Arterial Disease
Hospital Universitario Getafe0 个研究点目标入组 30 人开始时间: 2001年1月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 30
- 主要终点
- exercise tolerance
研究概览
简要总结
The study tests the use of a portable mechanical compression device (FM220, Flowmedic, USA) for the treatment of claudication and peripheral arterial disease.
Major endpoints are improved exercise tolerance and relevant blood pressure ratios
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 50 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •stable claudication with an absolute claudication distance >40 meters but <300
- •resting ABI in the affected limb <0.8
排除标准
- •presence of diabetes
研究组 & 干预措施
Active
Experimental
Active group receiving intermittent compression
干预措施: Intermittent Mechanical Compression (Device)
Control
Active Comparator
Standard Medical Treatment
干预措施: Control (Drug)
结局指标
主要结局
exercise tolerance
时间窗: 3 months
次要结局
- ankle-brachial index(3 months)
研究者
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