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Clinical trial

Safety Assessment, Instrumental and Perceived Efficacy 21 Days of Use at Home - Bepantol Derma Spray® Dermal and Gynecological Acceptability Assessment.

NCT03853512 is registered in ClinicalTrials.gov with Bayer as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Safety Assessment, Instrumental and Perceived Efficacy 21 Days of Use at Home - Bepantol Derma Spray® Dermal and Gynecological Acceptability Assessment.
Lead sponsor
Bayer
Phase
Phase 4
Overall status
Completed
Start date
February 12, 2019
Completion date
March 13, 2019
Enrollment
33 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

skin recovery