NCT06939907尚未招募不适用
Clinical Trial to Evaluate the Efficacy and Safety of Nexpowder™ for Diverticular Bleeding in the Lower Gastrointestinal Tract: A Prospective, Multi-Center, Single-Arm, Open-Label, Pilot Clinical Trial
Next Biomedical Co., Ltd.6 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年6月1日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 6
- 主要终点
- Rebleeding rate
研究概览
简要总结
Clinical Trial to Evaluate the Efficacy and Safety of Nexpowder™ for Diverticular Bleeding in the Lower Gastrointestinal Tract
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
- 19 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults aged 19 years or older at the time of screening
- •Patients diagnosed with diverticular bleeding
排除标准
- •Patients diagnosed with upper gastrointestinal bleeding
结局指标
主要结局
Rebleeding rate
时间窗: 30 days post treatment
30 days after successful endoscopic hemostasis
次要结局
- Hemostasis rate(Immediately after the procedure)
- Rebleeding rate(7 days post treatment)
研究者
研究点 (6)
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