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临床试验/NCT00481741
NCT00481741已完成4 期

A Prospective Randomized Controlled Efficacy and Safety Trial of the SafeSeal Hemostasis Patch Compared to Manual Compression for Achieving Vascular Hemostasis Following Percutaneous Coronary and Peripheral Intervention.

University of Rochester2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2007年5月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
150
试验地点
2
主要终点
Time to achieve hemostasis of femoral artery after arterial sheath removal

研究概览

简要总结

We seek to determine if the use of the SafeSeal(TM) topical hemostasis patch is associated with reductions in time to hemostasis and time to ambulation compared to standard manual compression after arterial sheath removal following percutaneous coronary and peripheral intervention. We further seek to assess the safety of the SafeSeal patch compared to manual compression.

详细描述

A variety of topical hemostasis pads containing procoagulant materials are currently available to accelerate hemostasis after removal of the arterial introducer sheath following coronary and peripheral arterial angioplasty procedures. The effectiveness and safety of these pads, however, remains poorly understood. A total of 150 patients undergoing coronary or peripheral vascular angioplasty through a 6 French arterial sheath will be randomized to sheath removal using manual compression alone or manual compression combined with use of the SafeSeal(TM) hemostasis patch. Sheaths will be removed at an activated clotting time (ACT) of <250 seconds, and patients will be kept at bedrest for 2 hours after hemostasis is achieved. The primary endpoint will be time to hemostasis. Secondary endpoints witll include time to ambulation and frequency of bleeding complications.

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

  • Patient ≥ 18 years old
  • Coronary or peripheral vascular intervention
  • 6 French arterial sheath used
  • Overnight hospitalization following procedure

排除标准

  • Hematoma or persistent bleeding around the vascular sheath
  • Previous AV fistula or pseudoaneurysm in the ipsilateral femoral artery
  • History of bleeding diathesis or coagulopathy
  • Hemoglobin level < 9 g/dl
  • Inability to ambulate at baseline
  • Known allergy to any of the materials used in the SafeSeal
  • Female patients known to be pregnant or lactating
  • Evidence of ongoing systemic or cutaneous infection
  • Uncontrolled blood pressure following PCI (systolic blood pressure > 180 or diastolic blood pressure >110)
  • Current enrolment in another ongoing investigational drug/device trial.

结局指标

主要结局

Time to achieve hemostasis of femoral artery after arterial sheath removal

时间窗: immediate

次要结局

  • vascular access-related bleeding complications(prior to hospital discharge)

研究者

申办方类型
Other

研究点 (2)

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