CTRI/2024/04/066514招募中Unknown
A Clinical Study to evaluate the efficacy of skin Renew Peptide Retinol Serum for skin Brightening - NI
Honasa Consumer Ltd.0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
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) Gender: Non-pregnant, non-lactating female aged between 25 to 45.
- •2) Subjects willing to give written informed consent
- •3) Women of childbearing potential must have a negative urine pregnancy test prior to study entry.
- •4) 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.
- •5) 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. Subjects who are pregnant, breast-feeding, or planning to become pregnant during the study.
- •2. Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition.
- •3. Have open sores or open lesions in the treatment area(s).
- •4. Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product.
- •5. Have participated in any interventional clinical trial in the previous 30 days.
- •6. Have a known sensitivity to any of the constituents of the test product.
- •7. Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including corticosteroids.
- •8. Have a history of alcohol or illegal drug or substance abuse, or suspected alcohol or illegal drug or substance abuse in the past 2 years.
研究者
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