A Clinical Study to Evaluate the effectiveness of Meso Odeon Face & Body Scrub-Turmeric & Yogurt for brightening
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 36
- 试验地点
- 1
研究概览
简要总结
A single blind one arm study.
Each participant entering the trial will be assigned to a regimen of investigational product with the below assessments.
- Skin Hydration with Corneometer (T0, 24hrs, T7days,T14days)
- TEWL for moisture barrier (T0, 24hrs, T7days,T14days)
- Blackheads by Visio (T0, T7days,T14days)
- Dark Spots by Visio(T0, T7days,T14days)
- Skin Color by Colorimeter (T0, T7days,T14days)
- Skin Melanin by Mexameter (T0, T7days,T14days)
- Dermat evaluation on a 5 point ordinal scale would be used for the even skin tone (T0, T7days,T14days)
- Dermat evaluation on a 5 point ordinal scale would be used for the skin radiance (T0, T7days,T14days)
- Dermat evaluation on a 5 point ordinal scale would be used for the skin tan (T0, T7days,T14days)
- HD Imaging with DSLR or Visioscan (T0 and T14)
Assessment Time: T0min, T+24hrs, T+7days, T+14 days
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 45.00 Year(s)（—）
入选标准
- •Gender: Male and Female with age 18-
- •Subjects with tanned and dull skin.
- •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
- •1.Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition.
- •2.Have open sores or open lesions in the treatment area(s).
- •3.Have any condition that, in the opinion of the investigator, would confound the safety and/or efficacy assessments of the product.
- •4.Have participated in any interventional clinical trial in the previous 90 days.
- •5.Have a known sensitivity to any of the constituents of the test product including sensitivities to (mention some of active ingredient’s name) 6.Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including corticosteroids.
- •7.Have not skin related issues.
研究者
Dr Robin Chugh
CCFT Laboratories