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临床试验/JPRN-UMIN000033507
JPRN-UMIN000033507已完成未知

A verification study of safety evaluation of the yeast materials long-term ingestion in humans: a randomized, double-blind, placebo-controlled, parallel study. - Safety evaluation of long-term ingestion of the yeast materials in humans.

Pharma Foods International Co., Ltd.0 个研究点目标入组 30 人开始时间: 2018年8月10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
30

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)A medical history of malignant tumor, heart failure or myocardial infarction. 2) Currently undergoing treatment for any of the following chronic diseases: atrial fibrillation, cardiac arrhythmia, liver failure, kidney failure, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 3) Subjects who currently taking medications (including herbal medicines) 4) Subjects who are allergic to medications and/or the test food related products. 5) Subjects who are pregnant, breast-feeding, or planning to become pregnant. 6) Subjects who are judged as ineligible to participate in the study by the physician.

研究者

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