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临床试验/JPRN-UMIN000053646
JPRN-UMIN000053646尚未招募Unknown

Effect of Daily Ingestion of Lactulose on Bone Density in Healthy Postmenopausal Women: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study. - Effect of Daily Ingestion of Lactulose on Bone Density in Healthy Postmenopausal Women.

Hokkaido Information University0 个研究点目标入组 150 人开始时间: 2024年2月25日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
150

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
45years-old 至 65years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1.Subjects with serious cancer, respiratory, hepatic, renal, cardiac, lung, gastrointestinal, blood, endocrine, metabolism diseases, and/or have serious medical history those disease. 2.Subjects with gastrointestinal disorders such as irritable bowel syndrome or inflammatory bowel disease. 3.Subjects with major surgical history relevant to the digestive system. 4.Subjects who regularly take medicine which would affect intestinal environment and/or bone metabolism. 5.Subjects who cannot abstain from taking functional foods (food for specified health uses, foods with function claims, foods with nutrient function claims) which affect intestinal environment, bone metabolism, and/or bone density, supplements which contain vitamin D3 and/or mineral. 6.Subjects who are at risk of having allergic reactions to drugs or foods, especially milk. 7.Subjects with lactose intolerance. 8.Subjects with a history of lumbar spine or hip surgery, and/or who have metal plates on their lumbar spine and/or hip. 9.Subjects who use pacemakers and/or defibrillators. 10.Subjects who currently participate in other clinical trials or participated within the last 4 weeks prior to the current study. 11.Subjects whose BMI is >=30 kg/m2. 12.Subjects who are ineligible due to physician's judgment.

研究者

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