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临床试验/JPRN-UMIN000047955
JPRN-UMIN000047955已完成未知

A Clinical Study to Evaluate Efficacy and Consumer Perception of a Test Material - A Clinical Study to Evaluate Efficacy and Consumer Perception of a Test Material

ION CORPORATIO0 个研究点目标入组 35 人开始时间: 2022年6月7日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
35

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
25years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • a) Female subject is pregnant, nursing, planning a pregnancy, or not using adequate birth control; b) Subject has eczema on the test sites; c) Subject has a sever itch with noticeable scratch (as determined by the LPN); d) Subject has hives; e) Subject uses a prescription itch reliever; f) Subject has received treatment with sympathomimetics, antihistamines, vasoconstrictors, non-steroidal anti-inflammatory agents, and/or systemic or topical corticosteroids within one week prior to initiation of the study; g) Subject has a history of acute or chronic dermatologic, medical, and/or physical conditions which would preclude application of the test material and/or could influence the outcome of the study; h) Subject is currently taking certain medications which, in the opinion of the Principal Investigator, may interfere with the study; i) Subject has known allergies to skin treatment products or cosmetics, toiletries, and/or topical drugs; j) Subject has a history of skin cancer, or is currently undergoing treatment for active cancer of any kind; k) Subject has insulin-dependent diabetes.

研究者

发起方
ION CORPORATIO

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