NCT01155401已完成不适用
Study of Incidence of Drug-induced Upper Gastrointestinal Bleeding
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
- 300
- 试验地点
- 1
- 主要终点
- Number and percentage of patients with drug-induced upper gastrointestinal bleeding
研究概览
简要总结
The purpose of this study is to determine and analyse the incidence, severity, risk factors and routine management of acute drug-induced upper gastrointestinal bleeding (UGIB) in the population of Russian patients
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 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
- •Established diagnosis of acute upper gastrointestinal bleeding, confirmed by presence of hematemesis/ coffee ground vomiting, melena, as well as other clinical or laboratory evidence of acute blood loss from the upper gastrointestinal tract
- •Written informed consent provided prior the start of participation in the study.
排除标准
- •Subjects who are unwilling or unable to provide informed consent.
结局指标
主要结局
Number and percentage of patients with drug-induced upper gastrointestinal bleeding
时间窗: About 1 year
次要结局
- Number and percentage of patients with each symptom and each Forrest class of upper gastrointestinal bleeding(About 1 year)
- Number and percentage of patients with each type of bleeding outcomes who received different types of hemostatic therapy(About 1 year)
- Number and percentage of patients with concomitant diseases contributing to drug-induced upper gastrointestinal bleeding and those who receive NSAIDs, antiplatelet agents, anticoagulants, steroids or combination therapy(About 1 year)
研究者
研究点 (1)
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