Trials / Completed
CompletedNCT07107854
EVALUATION OF THE EFFICACY OF COSMETIC PRODUCT IN ADULTS SUBJECTS WITH MILD TO MODERATE ACNE
EVALUATION OF THE EFFICACY OF COSMETIC PRODUCT IN ADULTS SUBJECTS WITH MILD TO MODERATE ACNE - USE TEST UNDER DERMATOLOGICAL CONTROL - MULTICENTER STUDY
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 110 (actual)
- Sponsor
- Cosmetique Active International · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Accepted
Summary
EVALUATION OF THE EFFICACY OF COSMETIC PRODUCT IN ADULTS SUBJECTS WITH MILD TO MODERATE ACNE. USE TEST UNDER DERMATOLOGICAL CONTROL. THE STUDY CONDUCTED IN POLAND AND MAURITIUS
Detailed description
Claims: * Improvement of acne * Improvement of skin smoothness parameters Objectives: To evaluate: * Its capacity to maintain the human face in good condition (cutaneous acceptability) by clinical examination under dermatological control; * their comedogenic potential by counting the retentional and inflammatory lesions by the dermatologist in charge of the study; * its smoothing effect by collecting polymer silicone skin's prints Silflo® and analysis using 3D Primos® Compact System * its capacity to improve skin elasticity using cutometer® * its capacity to maintain skin hydration using corneometer® * its effect on the skin state by clinical scoring by the dermatologist in charge of the study; * its effect on skin state by clinical auto scoring by the subjects; * their anti-acne effect by GEA score and AFAST (score B) by the dermatologist in charge of the study; * to illustrate their visual expected effect using ColorFace® and skincam®; * to evaluate the change of subjects' quality of life questionnaire (AI-ADL) from baseline to D84 and D168; * subjectively its cosmetic acceptability, properties, efficacy and future use by analysis of the subjects' answers to a subjective evaluation questionnaire
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | cosmetic: EFFACLAR ULTRA CONCENTRATED SERUM | Transparent solution (gel) |
Timeline
- Start date
- 2023-02-15
- Primary completion
- 2024-01-26
- Completion
- 2024-01-26
- First posted
- 2025-08-06
- Last updated
- 2025-08-06
Locations
1 site across 1 country: Poland
Source: ClinicalTrials.gov record NCT07107854. Inclusion in this directory is not an endorsement.