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Clinical Trial Summary

Determine the ability of the study material (personal lubricant) to cause sensitization by repeated topical application to the skin of humans under controlled patch test conditions.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Screening


Related Conditions & MeSH terms


NCT number NCT02297841
Study type Interventional
Source Church & Dwight Company, Inc.
Contact
Status Completed
Phase N/A
Start date November 2014
Completion date December 2014

See also
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