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临床试验/NCT01634438
NCT01634438已完成4 期

Low Versus High Dose Unfractionated Heparin in Patients Undergoing Angiography Via the Radial Artery

University of Alberta1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2008年7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
入组人数
49
试验地点
1
主要终点
radial artery occlusion

研究概览

简要总结

At present, coronary angiogram is usually performed either through an artery in your groin or wrist. An important limitation of the wrist approach is an increase rate of blockage of the wrist artery. It is possible that the dose of blood thinner (i.e. heparin) may decrease the risk of blockage. Early studies seem to suggest that higher dose is required to reduce the risk of this important complication. However, to date there has not been a definitive study to determine the most appropriate heparin dose for the prevention of this complication. The main goal of this study is to determine the appropriate heparin dose to prevent wrist artery blockage and to determine risk factors for developing such a complication.

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

  • Patients older than 18 years of age who were referred for either urgent or elective cardiac catheterization were eligible for the study if a normal Allen's test was demonstrated

排除标准

  • myocardial infarction with shock,
  • ST-elevation myocardial infarction,
  • patients undergoing planned percutaneous coronary intervention, and
  • patients in whom transradial approach is contraindicated such as hemodialysis patients

研究组 & 干预措施

low dose heparin

Experimental

30 units per kilogram of unfractionated heparin

干预措施: unfractionated heparin (Drug)

High dose heparin

Active Comparator

70 units per kilogram of unfractionated heparin (UFH) intravenously

干预措施: unfractionated heparin (Drug)

结局指标

主要结局

radial artery occlusion

时间窗: one month

The primary endpoint was radial artery occlusion defined as absence palpable radial artery with no flow as assessed by Doppler study

次要结局

未报告次要终点

研究者

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

Robert Welsh

Principal Investigator

University of Alberta

研究点 (1)

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