跳至主要内容
临床试验/CTRI/2025/09/094644
CTRI/2025/09/094644
尚未招募
Post Marketing Surveillance

A Clinical Study to Evaluate the moisturization potential of Deep Revitalise Balanced Barrier Creme- Sensitive skin

Honasa Consumer Limited1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年9月23日

概览

阶段
Post Marketing Surveillance
状态
尚未招募
发起方
Honasa Consumer Limited
入组人数
32
试验地点
1
主要终点
1. Change in Hydration

概览

简要总结

A single blind one arm study.

Each participant entering the trial will be assigned to a regimen of investigational product at marked Test product box and no product at the other box.

Assessment Time:

(Day 0 (T0min, T+30 mins)

Day 1 and Day 7)

Assessments:

  • Skin Hydration with Corneometer (Day 0 (T0min, T+30 mins) Day 1 and Day 7)

  • TEWL with Tewameter (Day 0 (T0min, T+30 mins) and Day 7)

  • IR imaging and sensitivity Score (0-4) (Day 0 (T0min, T+30 )

  • Erythema Index with Mexameter- redness (Day 0 and Day 7)

研究设计

研究类型
Pms
分配方式
Na
盲法
None

入排标准

年龄范围
20.00 Year(s) 至 35.00 Year(s)(—)

入选标准

  • Gender: Male or Female with age 20-
  • Subjects willing to give written informed consent 4) Women of child bearing potential must have a negative urine pregnancy test prior to study entry.
  • Are free of any systemic or dermatologic disorder, which, in the opinion of the investigator, will interfere with the study results or increase the risk of adverse events.
  • Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.

排除标准

  • Subjects who are pregnant, breast-feeding, or planning to become pregnant during the study.
  • Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition.
  • Have open sores or open lesions in the treatment area(s).
  • Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product.
  • Have participated in any interventional clinical trial in the previous 90 days.
  • Have a known sensitivity to any of the constituents of the test product.
  • Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e.,biologics), including corticosteroids.
  • Have not skin related issues.

结局指标

主要结局

1. Change in Hydration

时间窗: At T0min, T30min, T1 day and T7 Days

2. Change in TEWL

时间窗: At T0min, T30min, T1 day and T7 Days

3. IR ianging

时间窗: At T0min, T30min, T1 day and T7 Days

次要结局

  • Not Applicable(Not Applicable)

研究者

发起方
Honasa Consumer Limited
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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