NCT05632744已完成不适用
Evaluation of CG-100 Intraluminal Bypass Device
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 7
- 试验地点
- 2
- 主要终点
- Safety of the CG-100 Intraluminal Bypass Device
研究概览
简要总结
Evaluation of CG-100 Intraluminal Bypass device
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 22 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •(pre-operative):
- •Willing to comply with protocol-specified follow-up evaluations
- •22-75 (inclusive) years of age at screening
- •Diagnosed with colorectal cancer
- •Has been informed of the nature of the study, agrees to its provisions, and has provided written informed consent
排除标准
- 未提供
研究组 & 干预措施
CG-100 Intraluminal Bypass Device
Experimental
Subjects will be treated with CG-100 Intraluminal Bypass Device
干预措施: CG-100 Intraluminal Bypass Device (Device)
结局指标
主要结局
Safety of the CG-100 Intraluminal Bypass Device
时间窗: 10 days
Assessment of Serious Adverse Events
次要结局
- Safety of the CG-100 Intraluminal Bypass Device(4 weeks)
研究者
研究点 (2)
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