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临床试验/JPRN-UMIN000033180
JPRN-UMIN000033180已完成未知

A trial evaluating the efficacy of paprika oleoresin intake on bone metabolism: A randomized, placebo-controlled, double-blind, parallel-group comparison trial. - A trial evaluating the efficacy of paprika oleoresin intake on bone metabolism

Riken Vitamin Co., Ltd.0 个研究点目标入组 100 人开始时间: 2019年11月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
100

研究概览

简要总结

The percentage decrease of TRACP-5b at 24 weeks was significantly higher for paprika oleoresin than the placebo. There were no significant differences in sNTX or bone formation markers, although paprika oleoresin decreased each marker compared with the placebo.

研究设计

研究类型
Interventional

入排标准

年龄范围
40years-old 至 ot applicable(—)
性别
Female

入选标准

  • 未提供

排除标准

  • a) Subjects who are diagnosis with osteoporosis (Subjects who have less than 70% in total amount of bone mineral density for lumbar vertebra of YAM score). b) Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure or myocardial infarction. c) Currently undergoing treatment for any of the following chronic disease: cardiac arrhythmia, liver disease, kidney disease, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases. d) Subjects who take supplements, "Foods for Specified Health Uses," "Foods with Functional Claims," or "Foods with Nutrient Function Claims" related to bone metabolism such as calcium, vitamin D, vitamin K, magnesium, and isoflavones (including daidzein, genistein, equol, or etc.) more than once a week. e) Subjects who are currently taking medications (including herbal medicines) and supplements. f) Smoker g) Subjects who are allergic to medicines and/or the test food related products. h) Subjects who have been enrolled in other clinical trials within the last three months before the agreement to participate in this trial. i) Subjects who are judged as ineligible to participate in the study by the physician.

研究者

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