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临床试验/JPRN-UMIN000046570
JPRN-UMIN000046570已完成Unknown

Effects of consumption of the test food on bone density in healthy Japanese menopause women: a randomized, placebo-controlled, double-blind, parallel-group comparison study - Effects of consumption of the test food on bone density in healthy Japanese menopause women

ORTHOMEDICO Inc.0 个研究点目标入组 36 人开始时间: 2023年9月30日最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
36

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
20years-old 至 65years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1. Subjects who are osteoporosis (YAM score of total amount of lumbar vertebra is less than 70%) 2. Subjects who have taken medications for osteoporosis 3. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 4. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 5. Subjects currently undergoing treatment for any of the following chronic disease: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 6. Subjects who receive hormonal therapy 7. Subjects who take "Foods for Specified Health Uses", "Foods with Functional Claims", or other functional food/beverage in daily use 8. Subjects who take supplements, "Foods for Specified Health Uses", "Foods with Functional Claims", or "Food with Nutrient Function Claims" which may influence bone metabolism such as calcium, vitamin D or K, magnesium, lactic acid bacteria, or isoflavones (including daidzein, genistein, or equol) in daily use 9. Subjects currently taking medicines (include herbal medicines) and supplements 10. Subjects who are allergic to medications and/or the test-food-related products 11. Subjects who suffer from COVID-19 12. Subjects who have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 13. Subjects who are judged as ineligible to participate in the study by the physician

研究者

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