跳至主要内容
临床试验/CTRI/2024/12/077875
CTRI/2024/12/077875已完成Unknown

A consumer study to check the hyperpigmentation Activity of Asaya 2% Kojic Acid & 1% Alpha Arbutin Serum

Asaya1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年12月17日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
Percentage change in users observed change in

研究概览

简要总结

This is an observational, questionnaire based User test consumer study where the consumers would themselves evaluate the product efficacy after using the product for 4 weeks for its efficacy against Oil Reduction Potential of Asaya 2% Kojic Acid & 1% Alpha Arbutin Serum. 

Below data would be taken only at the end of the study as a subjective survey.

  1. Visibly fade dark spots

  2. Reduction in hyperpigmentation

  3. Fades blemishes

Done for 4 weeks on 100 healthy volunteers

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Voluntary man or women between 18 and 65 years.
  • Photo type III to V.
  • Having apparently healthy skin.
  • For whom the investigator considers that the compliance will be correct.
  • Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures.
  • Having signed a Consent Form.
  • Having valid proof of identity and age.

排除标准

  • Pregnant or nursing mothers 2.Dermatological infection or pathology on the level of studied area 3.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye) 4.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 5.Chronic illness which may influence the outcome of the study 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 food, cosmetic or therapeutic trial.

结局指标

主要结局

Percentage change in users observed change in

时间窗: At study end only (observation after 4 weeks)

visibly fade dark spots

时间窗: At study end only (observation after 4 weeks)

次要结局

  • Not Applicable(Not Applicable)

研究者

发起方
Asaya
申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

Dr Robin Chugh

CCFT Laboratories

研究点 (1)

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