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临床试验/JPRN-UMIN000051441
JPRN-UMIN000051441已完成Unknown

A verification study of the test product of skin improvement effect by application of test product: an open-label study - A verification study of the test product of skin improvement effect by application of test product

Wayo Women's University0 个研究点目标入组 17 人开始时间: 2023年6月23日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
17

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
18years-old 至 ot applicable(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. Subjects currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. Subjects who use or take "Foods for Specified Health Uses," or "Foods with Functional Claims" in daily 5. Subjects who are currently taking medications (including herbal medicines) and supplements 6. Subjects who are allergic to medicines and/or the test product related products 7. Subjects who have a medical history of allergy due to using cosmetics 8. Subjects who have inflammation symptoms at the site of application (elbow, knee, or heel) 9. Subjects who use skincare products on the site of application (elbow, knee, or heel) or receive skincare treatment during this trial 10. Subjects who are pregnant, lactating, or planning to become pregnant during this trial 11. 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 12. Subjects who are judged as ineligible to participate in this study by the physician

研究者

发起方
Wayo Women's University

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