Trials / Completed
CompletedNCT01909713
Tolerability of a Foaming Facial Cleanser and Moisturizer SPF 30 in a Pediatric Population (7-11) With Acne Prone Skin.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Galderma R&D · Industry
- Sex
- All
- Age
- 7 Years – 11 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the tolerability of Cetaphil® DermaControl™ Foam Wash and Moisturizer SPF 30 in pediatric subjects (7-11) with acne prone skin.
Detailed description
This was a open-label, single center study conducted in the United States that evaluated the tolerability of Cetaphil® DermaControl™ skin care products used at least once daily for 22 days in male and female subjects age 7 to 11 with acne prone skin. There were 4 visits during the course of the study: screening (within 7 days of visit 1), visit 1(baseline /day1), visit 2 (day 8), and visit 3 (day 22/exit). Tolerability assessments were performed by a board certified dermatologist at all visits. Subjects completed the baseline skin care regimen questionnaire at visit 1. Hydration assessments were competed at visits 1, 2, and 3. A subject satisfaction questionnaire was completed at visit 3. Adverse event assessments were conducted for all subjects at every clinic visit after informed consent/assent was signed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Facial Cleanser and Moisturizer SPF 30 | Cetaphil® DermaControl™ Foam Wash and Moisturizer SPF 30 |
Timeline
- Start date
- 2013-05-01
- Primary completion
- 2013-06-01
- Completion
- 2013-06-01
- First posted
- 2013-07-26
- Last updated
- 2022-08-23
- Results posted
- 2014-03-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01909713. Inclusion in this directory is not an endorsement.