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临床试验/NCT01564888
NCT01564888已完成4 期

Prevention of Radial Artery Occlusion: Prophylactic Hyperperfusion Evaluation Trial

Total Cardiovascular Solutions3 个研究点 分布在 2 个国家目标入组 3,000 人开始时间: 2011年1月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
3,000
试验地点
3
主要终点
30 day radial artery occlusion

研究概览

简要总结

Evaluating the effect of ulnar artery compression while pressing on radial artery to stop bleeding, in maintaining radial artery potency, after cardiac catheterization through the radial artery. We prospectively plan to compare 3000 patients referred for cardiac catheterization, randomized into two groups, one group receiving radial artery compression for stopping bleeding, in a standard fashion following best practices, and the other group receiving radial artery compression using standard best practices and ulnar artery compression. Radial artery status will be evaluated in 24 hours and 30 days of the procedure to evaluate its potency, using plethysmography.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients referred for diagnostic cardiac catheterization.

排除标准

  • previous ipsilateral radial artery puncture, warfarin therapy, absence of intact palmar collateral circulation, scleroderma, ipsilateral radial artery surgery, lone upper extremity (contralateral upper extremity amputation), ipsilateral upper extremity chronic pain.

结局指标

主要结局

30 day radial artery occlusion

时间窗: 30 days

Evaluation of radial artery patency using plethysmography

次要结局

  • hand ischemia(2 hours)

研究者

发起方
Total Cardiovascular Solutions
申办方类型
Other
责任方
Sponsor

研究点 (3)

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