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临床试验/JPRN-UMIN000032555
JPRN-UMIN000032555已完成未知

A clinical study to evaluate the anti-obesity effect of capsules containing noni fruit powder. - A clinical study to evaluate the anti-obesity effect of capsules containing noni fruit powder.

Soiken Inc.0 个研究点目标入组 120 人开始时间: 2019年8月31日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
Soiken Inc.
入组人数
120

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 55years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subject who has a mental disease such as depression, schizophrenia, epilepsy and bulimia nervosa. 2) Subject who has allergic disease, cardiovascular, respiratory, thyroid gland malfunction, diabetes, heart disease, heart disease, gout or sleep disorder. 3) Subject who takes regularly medicinal drugs or medicines having an effect on the weight. 4) Subject who has the possibility of developing allergic symptoms by the test food (noni allergy). 5) Subject who has a snacking habit that influence the evaluation of the effects of the test food. 6) Female subject who is pregnant or may be pregnant during the study. 7) Female subject who is in the lactation during the study. 8) Subject who took blood samples of 200 ml or more within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood). 9) Subject who participated in other clinical trials within the past 4 months or currently participating in other clinical trials or planning to participate in other clinical trials during the examination period. 10) Subject deemed unsuitable by the investigator.

研究者

发起方
Soiken Inc.

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