跳至主要内容
临床试验/CTRI/2017/08/009239
CTRI/2017/08/009239招募中不适用

Evaluation of dermatological safety of investigational products by 24hrs patch test under complete occlusion on healthy human subjects.

Dabur India Limited1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2014年1月30日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
24
试验地点
1
主要终点
The objective of this study is to evaluate the dermatological safety of the investigational products on healthy human subjects

研究概览

简要总结

Objective:

Theobjective of this study is to evaluate the dermatological safety of theinvestigational products on healthy human subjects.

Subject Population:

24 healthy human volunteers.

Duration of study:

Approximately 9 days for each volunteer

The required quantity of the sample will be put on the upper back of  subjects and closed with IQ chambers prefixed on tape.

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 removal.

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 age group
  • 55 years •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 •Hyper sensitivity to any component of the tested products •Athletes and subjects with history of excessive sweating •Cutaneous disease which may influence the study result •Chronic illness which may influence the cutaneous state.
  • •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

The objective of this study is 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

申办方类型
Other [Healthcare and FMCG]

研究点 (1)

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