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临床试验/JPRN-UMIN000044208
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Safety evaluation of long term intake of test supplement - Safety evaluation of long term intake of test supplement

FANCL Corporation0 个研究点目标入组 60 人开始时间: 2021年5月16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
60

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
All

入选标准

  • 未提供

排除标准

  • 1. Subjects who are judged as unsuitable for the study based on the results of clinical laboratory test or cardiopulmonary function. 2. Subjects who have allergy related to this study. 3. Subjects who have diseases requiring continuous medication, or serious medical history who needed medication. 4. Subjects whose clinical laboratory tests, blood pressure, and physical measurements before intake of trial supplements are significantly out of the standard values. 5. Subjects who have participated in other clinical studies. 6. Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. 7. Subjects who are judged as unsuitable for the study based on the answers of background survey. 8. Subjects who are judged as unsuitable for the study by the investigator for other reasons.

研究者

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