CTRI/2012/04/002579已完成未知
Evaluate the safety and possible allergenicity of C.L.A.I.M.S. chambers using Human Repeat Insult Patch Test (HRIPT) technique in Men and Women
CLAIMS Pvt Ltd0 个研究点目标入组 200 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 200
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
入选标准
- •1.Voluntary men and women based on diagnostic patch test.
- •2.Between 18 and 65 years.
- •3.Phototype IV and lower (Phototype IV- Moderate brown skin which rarely burns and tans with ease. Phototype III (Lower) - White skin which sometimes burns, difficult to tan).
- •4.Having apparently healthy skin on studied area.
- •5.Willingness to discontinue the use of cleansing and/or cosmetic products in the treatment areas during the course of the study.
- •6.For whom the Investigator considers that the compliance will be correct.
- •7.Cooperating, informed of the need and duration of the examinations, and ready to comply with protocol procedures.
- •8.Having signed a Consent Form and will be once informed orally and in writing of all information concerning the study procedures and study objectives.
- •9.Willingness to avoid intense UV exposure (sun or artificial UV) on test site, during the course of the study.
- •10.Willingness to avoid water contact (i.e.: swimming) or activity which cause sweating (i.e.: exercise, saunaâ?¦), during the course of the study.
- •11.Ready to wear loose cotton clothes.
排除标准
- •1.People who have a job involving water contact or a job which causes perspiration. (Routine work can be done. No carrying out activities like excessive/brisk walking, exercising etc. which will lead to excessive sweating).
- •2.Scars, hairs or tattoo on the studied area.
- •3.Pregnant women (as confirmed by UPT) and lactating women.
- •4.Hypersensitivity allergy antecedent to any cosmetic product in general or raw material by history.
- •5.Any clinically significant systemic or cutaneous disease, which may interfere with study treatments or procedures.
- •6.Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month).
- •7.Subject in an exclusion period or participating in another similar cosmetic or therapeutic trial.
- •8.Volunteers with any skin condition that may cause interference with interpretation of the reactions or volunteers with past or present history of a photosensitive dermatosis.
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