Clinical Trials Directory

Trials / Completed

CompletedNCT05821296

Evaluation of Efficacy and Tolerance of Crystal Peel in the Treatment of Adults Presenting Facial Mild Acne

Evaluation of the Efficacy and Tolerance of Crystal Peel (a Salicylic Acid Based Peel) in the Treatment of Acne

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Dermosciences France · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The goal of this interventional, confirmatory and post market study is to evaluate the efficacy and clinical performance of Crystal Peel in adults suffering mild facial acne vulgaris. The principal and secondary aims are: * Principal aim: to evaluate the efficacy and clinical performance of Crystal Peel, a salicylic-based peel, for the treatment of acne by lesions counting (front, 2 cheeks, the chin above the jaw line (excluding the nose)) using both visual observation and palpation. * Secondary aims: pores and texture analysis, visual effect (Standardized anonymized photographs, investigator global assessment, patient global assessment, local and overall tolerance of the Crystal Peel, subject's self-evaluation and potential adverse events collection. The primary endpoint of the study will be an objective counting of the acne lesions performed on every visit.

Detailed description

Total lesions will be defined as the sum of inflammatory lesions (papules and pustules), non-inflammatory lesions (whiteheads and blackheads) and other acne lesions (nodules).

Conditions

Interventions

TypeNameDescription
DEVICECrystal Peel3 applications performed by a dermatologist.

Timeline

Start date
2023-01-23
Primary completion
2023-06-07
Completion
2023-06-07
First posted
2023-04-20
Last updated
2024-10-15
Results posted
2024-10-01

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT05821296. Inclusion in this directory is not an endorsement.