JPRN-jRCTs052190096进行中（未招募）未知
Postoperative endovascular intervention for false lumen for aortic dissection - FL intervention
Matsuda Hitoshi0 个研究点目标入组 15 人开始时间: 2020年1月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 15
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 ot applicable（—）
- 性别
- All
入选标准
- •Patients who had past history of undergoing the surgery for aortic dissection.
- •Patients who developed aortic dilation more than 45mm in thoracic aortic aneurysm or more than 40mm in abdominal aortic aneurysm.
- •Patients who developed rapid aortic dilation more than 3mm in 6 months or more than 5mm in 12months.
排除标准
- •Patients who had systemic infection that may increase the risk of device-related infection.
- •Patients who are allergic to the material of the device.
- •Pregnant women, lactating women or women who cannot agree on contraception during participating in this study.
研究者
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