EUCTR2006-006873-25-FR进行中（未招募）1 期
A randomised, multicentre, single-blind, phase IV study, of the efficacy, safety and acceptability of MoviPrep® versus Colopeg® in colonoscopy preparation.
orgine Pharma0 个研究点目标入组 0 人开始时间: 2007年2月15日最近更新:
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相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
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
- •1.The patient's written informed consent must be obtained prior to inclusion.
- •2.Male or female, outpatients between 18 and 85 years old with an indication to colonoscopy.
- •3.Willing and able to complete the entire procedure and to comply with study instructions.
- •4.Females of childbearing potential must employ an adequate method of birth control.
- •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
- •1.Age < 18 or > 85 years old,
- •3.Suspected intestinal occlusion or perforation,
- •4.Toxic megacolon with severe inflammation conditions of intestinal tract (patients with Crohn's Disease or Ulcerative Colitis included),
- •5.Gastroparesis,
- •6.Congestive heart failure NYHA III or IV,
- •7.Documented Carcinoma or any other colic disease leading to a fragile mucosa,
- •8.Documented severe renal insufficiency history
- •9.Known hypersensitivity to MoviPrep®, Colopeg® or to any of their components (PEG, ascorbic acid etc.),
- •10.Known deficiency in G6PD and/or phenylcetonuria,
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