JPRN-jRCT1051220043已完成未知
A prospective, randomized and endoscopist-blinded trial to evaluate comparable efficacy of a 1-L PEG and ascorbic acid with sennoside versus a 2-L PEG and ascorbic acid for bowel preparation - Senno trial
Fukuda Takashi0 个研究点目标入组 344 人开始时间: 2022年6月10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
- 344
研究概览
简要总结
The 1L-PEG/AS regimen was comparable to the 2L-PEG/A regimen in terms of BP adequacy, requiring lesser BP solution volumes, with better patient tolerance.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 <= 85age old（—）
- 性别
- All
入选标准
- •1) patients who were scheduled for elective colonoscopy
- •2) patients who aged over 20 years old and under 85 years old
- •3) patients who were able to fill in the informed consent form for participation
排除标准
- •1) severe heart failure (NYHA class III or IV)
- •2) severe hepatic failure (Child-Pugh C)
- •3) active inflammatory bowel disease
- •4) dementia
- •5) allergy to Moviprep or sennoside
- •6) advanced colorectal cancer
- •7) intestinal resection
- •8) past history of participance in this study
研究者
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