EUCTR2009-013294-18-HU进行中（未招募）不适用
Magnesiumsulfate in the prevention of post-ERCP pancreatitis – a prospective randomized, placebocontrolled multicenter study
niversity of Szeged, First Department of Internal Medicine0 个研究点目标入组 802 人开始时间: 2014年1月13日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 802
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Adult (= 18 years of age) patients (male and female) with a medical indication for a diagnostic or therapeutic
- •endoscopic retrograde cholangiopancreatography (ERCP).
- •Written informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Known allergy or intolerance to one of the medicaments utilized in the study or their ingredients
- •Participation in another clinical study during the previous four weeks
- •Pregnancy and breast feeding
- •Acute pancreatitis
- •Renal insufficiency = stadium 4 (K/DOQI)
- •Hyperthyreoidism
- •Symptomatic Bradycardia <35 bpm
- •Atrioventricular block > 1° or other cardial conduction defects
- •Myasthenia gravis
- •Liver cirrhosis Child C
- •Any apparent coagulopathy
- •Kidney stone diathesis (calcium-magnesium-ammonium-phosphate stones)
- •Mental impairment, addicitve or other disorders leading to the patients inability to understand the scope and
- •possible consequences of a participation in the clinical trial
- •Magnesium medication within 14 days before the procedure
- •Inability to give informed consent
研究者
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