NCT01292915已完成不适用
Survey of Non-Variceal Upper Gastro Intestinal Bleeding in Vietnamese Patients
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 1,044
- 试验地点
- 1
- 主要终点
- Rebleeding (within 7 days from the Non-Variceal Upper Gastro Intestinal Bleeding (NVUGIB) episode)
研究概览
简要总结
The main aim of the study is to describes the outcomes of patients with Upper Gastrointestinal Bleed (UGIB) in a real-life setting. Additionally analyse assessed predictors of outcome, including the impact of hemostatic endoscopic and pharmacologic therapies.
详细描述
MSD
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- •Adult patients (>=18yrs) admitted to the hospital, or inpatients admitted for another reason, presenting with overt non-variceal upper GI bleed manifesting as hematemesis/coffee ground vomiting, melena, hematochezia...
- •Evidence that an upper GI endoscopy was performed
排除标准
- •GI bleeding not from NVUGIB
结局指标
主要结局
Rebleeding (within 7 days from the Non-Variceal Upper Gastro Intestinal Bleeding (NVUGIB) episode)
时间窗: 7 days
次要结局
- Surgery due to re-bleeding(7 days)
- Mortality due to bleeding(7 days)
- Rebleeding in high risk peptic ulcer patients(7 days)
研究者
研究点 (1)
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