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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01888887
Other study ID # GLI.04.SRE.US10236
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 2012

Study information

Verified date June 2013
Source Galderma R&D
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Determine if Cetaphil Daily Facial Cleanser is a contact sensitizer or irritant to the skin


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date
Est. primary completion date February 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Not currently under a doctor's care - Free of dermatological or systemic disorder which would interfere with the results - Free of any acute or chronic disease - Will complete a preliminary medical history form and are in general good health - Can read, understand, and sign informed consent Exclusion Criteria: - Under 18 years old - Currently under doctor's care - Currently taking any medication - History of acute or chronic disease - Diagnosed with chronic skin allergies - Pregnant or lactating

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cetaphil Daily Facial Cleanser


Locations

Country Name City State
United States AMA Laboratories New City New York

Sponsors (1)

Lead Sponsor Collaborator
Galderma R&D

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary area of erythema and edema to test reaction of skin to product 9 consecutive 24hr exposures for every Monday, Wednesday, and Friday for 3 consecutive weeks will be conducted to test the reaction of the skin to the test product 3 consecutive weeks
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