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临床试验/NCT02857738
NCT02857738已完成不适用

Sun Protection Factor (SPF) - Static and Water Resistant Assay

Bayer0 个研究点目标入组 12 人开始时间: 2015年5月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Bayer
入组人数
12
主要终点
Evaluation of water resistant SPF in accordance to ISO 24444

研究概览

简要总结

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female of an age of 18 to 70 years inclusive;
  • Fitzpatrick Skin Type I, II and/or III for SPF testing;
  • Good health as determined from the CRO Subject History Form (SHF);
  • Signed and dated Informed Consent Form;
  • Signed and dated Health Insurance Portability and Accountability Act (HIPAA) Form;
  • An unambiguous minimal erythema dose (MED).

排除标准

  • 未提供

研究组 & 干预措施

SPF evaluation

Experimental

Subjects with Good health as determined from the CRO Subject History Form (SHF) and Fitzpatrick Skin Type I, II and/or III were included for SPF testing.

干预措施: BAY 987519 (Drug)

SPF evaluation

Experimental

Subjects with Good health as determined from the CRO Subject History Form (SHF) and Fitzpatrick Skin Type I, II and/or III were included for SPF testing.

干预措施: SPF 15 Control (Drug)

结局指标

主要结局

Evaluation of water resistant SPF in accordance to ISO 24444

时间窗: 16-24 hrs post exposure

次要结局

未报告次要终点

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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