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.
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