CTRI/2024/01/061162已完成4 期
A Clinical Study to evaluate the 8-hour moisturization potential of Multiple SaliguardSamples at concentration 1.5% - NI
Salicylates & Chemicals Pvt. 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
- 4 期
- 状态
- 已完成
- 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: Male or Female with age 18-40
- •2) Subjects willing to give written informed consent
- •3) Women of child bearing 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
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
- •5. Have participated in any interventional clinical trial in the previous 90 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 not skin related issues
研究者
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