DRKS00031251已完成不适用
Evaluation of the efficacy and safety of the MYNX CONTROL™ vascular closure device for achieving primary haemostasis after arterial femoral access following peripheral arterial interventions compared to the FemoSealTM vascular closure device
niversitäts-Herzzentrum Campus Bad Krozingen - Uniklinikum Freiburg0 个研究点目标入组 273 人开始时间: 2023年6月22日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 273
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 100 Years（—）
- 性别
- All
入选标准
- •Patients with peripheral arterial interventions performed at the University Heart Centre Campus Bad Krozingen
- •Patients in whom the MYNX CONTROL™ or FemoSealTM closure system was used
排除标准
- •Patients in whom no closure device or another closure device has been used
研究者
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