NL-OMON41463已完成不适用
Percutaneous access in Endovascular Repair versus Open - PiERO
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 137
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 至 99（—）
入选标准
- •Patients must be physically and mentally capable of giving consent for randomised femoral access and data storage,
- •in the possession of an aneurysm of the abdominal aorta with a diameter of at least 55 millimetres (or growth of 5 millimetres or more in half a years* time),
- •suitable for bifurcated endovascular repair through two femoral access sites, without additional access needed.
排除标准
- •Patients with extreme atherosclerosis (more than half (1/2) of the circumference of the CFA)
- •Previous common femoral artery surgery.
- •Patients treated with an aorto-monoiliacal device implanted, followed by a femorofemoral cross-over.
- •Patients in need for more than two femoral accesses (brachial or carotid).
- •Patients treated with a Nellie device (Endologics)
研究者
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