Clinical Trials Directory

Trials / Completed

CompletedNCT06942403

In-use Tolerance and Efficacy Study Under Dermatological Control of an Anti-aging Cream (Split Face) Post Facial Superficial Rejuvenation Procedures, After re Epidermization

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Pierre Fabre Dermo Cosmetique · Industry
Sex
All
Age
35 Years – 70 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to assess the dermatological tolerance of the investigational product "Crème visage Product code: RV4983A / Formula code: LA3365" after 95 days for subjects post peeling and LASER and 176 days for subjects post injections of once daily use at the evening on the half face, under normal conditions of use, on 66 subjects. This study will be conducted as a national, monocentric, open trial. Planning of the visits: * Visit 1: Inclusion (Day 1) - The subjects undergo their procedure (peeling, LASER or injections). * Home application of the associated product 1 period: Day 1 to Day 7 * Visit 2: intermediate visit (Day 8) subjects received investigational product and associated product 2; * Visit 3, 4, and 5: Intermediate visit (Day 37, Day 66 and Day 95\*), \*the final visit for the subjects post peeling and LASER * Visit 6\*\*: End of study (Day 176), \*\* for subjects post injections

Conditions

Interventions

TypeNameDescription
OTHERAssociated product 1 : RV2666CApplied twice a day minimum during 7 days (from Day 1 to Day 7)
OTHERAssociated product 2 MORNING : RV5000AApplied in the mornings from Day 8 to Day 95 or Day 176\* \* for subjects post injections
OTHERTest product : RV4983AApplied once a day, at the evening. Avoid contact with eyes. If sensations of discomfort appear, allow more time between applications. * From Day 8 to Day 95 (87 days) for post LASER and post peeling subjects * From Day 8 to Day 176 (169 days) for post-injections subjects
OTHERAssociated product 2 EVENING: RV5000AApplied in the evenings from Day 8 to Day 95 or Day 176\* \* for subjects post injections

Timeline

Start date
2023-09-27
Primary completion
2024-03-26
Completion
2024-03-26
First posted
2025-04-24
Last updated
2025-04-24

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT06942403. Inclusion in this directory is not an endorsement.