St. Petersburg, Florida, 33714, United States
NCT Number: NCT02877511
Supervised Outdoor-Use Test For Sunscreen Products in Adults
To assess the safety of a sunscreen product under supervised outdoor-use conditions
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Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Subject must be healthy, males or females between 18 to 65 years of age with no medical conditions of the skin.
- Subjects must have Fitzpatrick Skin Type I, II, III or IV.
- Subjects must agree to restrict their sun exposure activities for at least five days immediately preceding participation in the study.
Exclusion criteria
- Subjects must not have actinic keratoses, skin cancer, psoriasis, eczema, or any other acute or chronic skin conditions.
- Subjects must not have visible erythema, blistering, or peeling that would indicate recent sunburn as determined by the baseline skin evaluation.
- Subjects must not have significantly tanned skin.
Treatment and study plan
BAY987517
DrugApplied liberally to the skin (Formulation: Y73-161
Sunscreen Lotion (Y65-110)
DrugApplied liberally to the skin
Primary outcomes
-
Skin response to sun exposure according to the Skin Evaluation Response Scale from 0 to 3
Time frame: From the beginning of the study until 24 hours after study
Sponsors and collaborators
Lead sponsor
Bayer
Industry
Registry information
Important dates
- Study start
- 2016
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Aug 24, 2016
- Registry last updated
- Dec 13, 2018
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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