JPRN-UMIN000044272已完成未知
A randomised, double-blind, placebo-controlled crossover clinical trial on the effect of lactulose on improving the intestinal environment. - A clinical trial on the effect of lactulose on improving the intestinal environment.
Megurodoori Gastrointestinal Surgery Internal Medicine Clinic0 个研究点目标入组 36 人开始时间: 2021年5月20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
- 36
研究概览
简要总结
Ingestion of 4 g of lactulose for 3 days increased fecal bifidobacterial occupancy.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 65years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Subjects with severe hepatic, renal, heart, gastrointestinal, cerebrovascular, endocrine, metabolic or infection diseases. 2) Subjects with the history of gastrointestinal resection. 3) Subjects with gastrointestinal dysfunction such as irritable bowel syndrome or inflammatory bowel disease. 4) Subjects who use medicines or supplements that may influence feces frequency; e.g. antibiotics, probiotics, laxatives, antidiarrheals, fibers. 5) Subjects with milk allergy or lactose intolerance. 6) Subjects who participate another study. 7) Subjects who are judged inappropriate for the study by the investigator or the physician.
研究者
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