The purpose of this test is to evaluate the sensitizing potential of a personal lubricant, as a result of repeated occlusive patch. The intervention will be applied for a total of 9 induction applications, followed by an approximately 2 week rest period, then followed by a 24-72 hour Challenge applications.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SCREENING
Masking
NONE
Enrollment
222
Harrison Research Laboratories, Inc.
Union, New Jersey, United States
Number of Patients That Showed Sensitization Reaction to the Test Material at Challenge
Time frame: 24, 48 and 72 hours after patch application
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.