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临床试验/CTRI/2019/04/018464
CTRI/2019/04/018464已完成未知

To Evaluate Dermatological Safety of Investigational Products by 24 Hours Patch Test Under Complete Occlusion on Adult Healthy Human Subjects with Non-Sensitive and Sensitive Skin

Dabur India Limited0 个研究点目标入组 24 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
24

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. Healthy male and female subjects (1:1 ratio) in the age group of 18-65 years (both age inclusive) with non-sensitive skin
  • 2. Subjects scoring less than or equal to 30 for Section 2- Sensitive v/s Resistant skin in modified Dr. Baumannâ??s skin type questionnaire. Please see detail annexure II
  • 3. Subjects representing with normal, oily, dry and combination skin type in equal ratio.
  • 4. Subjects with normal Fitzpatrick skin type III to V.
  • 5. Female subjects with child bearing potential willing to undergo Urine Pregnancy Test.
  • 5. Subjects free from excessive hair, cuts, wounds, irritation symptoms, abrasion or any other skin condition which may interfere in the study results.
  • 6. Subjects willing to give voluntary written informed consent.
  • 7. Subjects willing to maintain the patch test in position for 24 hours.
  • 8. Subject having not participated in a similar investigation in the past two weeks.
  • 9. Subjects willing to come for regular follow up visits.
  • 10. Subjects ready to follow instructions during the study period.

排除标准

  • 1. Infection, allergy on the tested area.
  • 2. Skin allergy antecedents or atopic subjects.
  • 3. Subjects with known hypersensitivity to any of the study products or constituents.
  • 4. Subjects with any significant skin pathology in the investigational area
  • 5. Athletes and subjects with history of excessive sweating.
  • 6. Cutaneous disease which may influence the study result.
  • 7. Subjects using any topical or systemic treatment that could interfere with the study treatments/assessments within the last 4 weeks prior to participation in the study and during the study.
  • 8. Subjects on oral corticosteroid
  • 9. Subjects participating in any other cosmetic or therapeutic study.
  • 10. Female subjects who are pregnant or lactating.
  • 11. Any history of underlying uncontrolled medical illness including diabetes, liver disease or history of alcoholism, HIV or any other serious medical illness.

研究者

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