Repeat Insult Patch Test of Skin Irritation/Sensitization for Cetaphil Dermacontrol Oil Control Moisturizer SPF 30
Cetaphil Dermacontrol Oil Control Moisturizer SPF 30- 100 Human Subject Repeat Insult Patch Test Skin Irritation/Sensitization Evaluation (Semi-occlusive Patch)
1 other identifier
interventional
100
0 countries
N/A
Brief Summary
Determine if Cetaphil DermaControl Oil Control Moisturizer SPF 30 proves to be a contact sensitizer or irritant in certain individuals
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2013
CompletedFirst Submitted
Initial submission to the registry
June 21, 2013
CompletedFirst Posted
Study publicly available on registry
June 27, 2013
CompletedJuly 29, 2022
June 1, 2013
1 month
June 21, 2013
July 28, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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
Study Arms (1)
Cetaphil DermaControl Oil Control Moisturizer SPF 30
EXPERIMENTALAll subjects receive Cetaphil DermaControl Oil Control Moisturizer SPF 30
Interventions
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Galderma R&Dlead
Study Officials
- PRINCIPAL INVESTIGATOR
Mayya Tastene, MD
AMA Laboratories
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 21, 2013
First Posted
June 27, 2013
Study Start
December 1, 2012
Primary Completion
January 1, 2013
Last Updated
July 29, 2022
Record last verified: 2013-06