NCT07668687招募中不适用
European Multi-Centre Castor™ and Cratos™ Branched Endovascular Arch Repair Registry
Shanghai MicroPort Endovascular MedTech（Group）Co., Ltd4 个研究点 分布在 2 个国家目标入组 100 人开始时间: 2025年9月12日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 100
- 试验地点
- 4
研究概览
简要总结
The Castor™ and Cratos™ Branched Aortic Stent Graft Systems are medical devices designed for the minimally invasive endovascular treatment of thoracic aortic pathologies in the descending aorta. The goal of this multi-centre retrospective and prospective observational registry study is to capture the short-, medium- to long-term safety and performance data of how Castor™ and Cratos™ stent-grafts work in real-world settings (everyday medical practice). The aim is to study approximately 100 patients in European hospitals, with competitive enrollment.
详细描述
The CEDAR registry is a post-market clinical study with retrospective and prospective enrollment and retrospective and prospective data collection.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Implantation of a Castor™ or Cratos™ single branch endoprothesis with incorporation of the left subclavian artery
- •Age >18 years
排除标准
- •Patients allergic to the materials of the device;
- •Patients with severe or potentially systemic infections that increase the chance of graft infection;
- •Minors and pregnant women;
- •Branch for other supra-aortic vessels than the LSA
- •Rejection of participation.
研究者
研究点 (4)
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