Clinical Trials Directory

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

TypeNameDescription
DRUGFacial Cleanser and Moisturizer SPF 30Cetaphil® 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.