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临床试验/CTRI/2016/07/007064
CTRI/2016/07/007064已完成不适用

Evaluation of dermatological safety of investigational products by primary irritation patch test on healthy human volunteers of varied skin types.

ITC Life Science and Technology Centre1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2015年11月18日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24
试验地点
1
主要终点
To evaluate the dermatological safety of the investigational products on healthy human subjects

研究概览

简要总结

Objective:

The Objective of the study is to evaluate the dermatological safety of investigational products on healthy human subjects

Subject Population:

24 healthy human volunteers (Male and Female 1:1) with skin type 1:1:1:1 ratio ( Oily,Dry,Normal and Combination)

Duration of study:

Approximately 9 days for each volunteer

The patch will be applied at the test site of study subjects starting with the lower edge of the patch system and slowly pressing upwards till the top edge in order to squeeze out the air.

This patch will then be applied on the test site i.e. between the scapulae and waist of the subjects. The patch will be kept for 24 hours. After which the patches will be removed and the first observation will be made at 30 minutes of patch removal (0 hr. observation). The further observations will be at 24 hr and 1 week of patch

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • •Subjects in the age group
  • 55 years (both the ages inclusive). •Healthy male & female subjects. •Subjects with Fitzpatrick skin type III to V. •Subjects willing to give a written informed consent. •Subjects willing to maintain the patch test in position for 24 hours. •Subject having not participated in a similar investigation in the past two weeks. •Subjects willing to come for regular follow up visits. •Subjects ready to follow instructions during the study period.

排除标准

  • •Infection, allergy on the tested area.
  • •Skin allergy antecedents or atopic subjects.
  • •Athletes and subjects with history of excessive sweating.
  • •Cutaneous disease which may influence the study result.
  • •Subjects on oral corticosteroid.
  • •Subjects participating in any other cosmetic or therapeutic study.
  • •Any history of underlying uncontrolled medical illness including diabetes, liver disease or history of alcoholism, HIV or any other serious medical illness.

结局指标

主要结局

To evaluate the dermatological safety of the investigational products on healthy human subjects

时间窗: 0hr,24hr and 7days post patch removal

次要结局

未报告次要终点

研究者

发起方
ITC Life Science and Technology Centre
申办方类型
Other [fmcg]

研究点 (1)

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