JPRN-UMIN000004592已完成未知
Multicenter, placebo-controlled randomized trial for prevention of post ERCP pancreatitis with Risperidone - Tokyo P3R-2
Faculty of Medicine, University of Tokyo0 个研究点目标入组 500 人开始时间: 2010年12月1日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 500
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
- 20years-old 至 80years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Patients with a history of ERCP. Patients with acute pancreatitis which need fasting therapy. Patients who have disseminated intravascular coagulation, sepsis, or acute circulatory failure. Patients with more severe disturbance of consciousness than Japan Coma Scale1-1. Patients who have severe heart disease, hepatic insufficiency, renal dysfunction, endocrine disease, or gastrointestinal tract disturbance. Pregnant or breast-feeding women. Women who have possibility of pregnancy or who are not willing to avoid pregnancy during the study. Patients who are treated with risperidone. Patients with severe hypersensitivity to risperidone Patients with mental illness or depression, who need drug therapy or can not comply with the protocol. Patients with Parkinson's disease or parkinsonism. Patients who have received banned drug within 2 weeks before ERCP Patients with chronic pancreatitis Patients who are judged inappropriate by chief (responsive) medical examiner
研究者
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