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

NCT ID: NCT06942403

Last Updated: 2025-04-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 66 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-09-27
• Study Completion Date: 2024-03-26

Brief 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

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Treated group (hemiface)

Group Type: EXPERIMENTAL

Associated product 1 : RV2666C

Intervention Type: OTHER

Applied twice a day minimum during 7 days (from Day 1 to Day 7)

Associated product 2 MORNING : RV5000A

Intervention Type: OTHER

Applied in the mornings from Day 8 to Day 95 or Day 176*

• for subjects post injections

Test product : RV4983A

Intervention Type: OTHER

Applied 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

Control group (hemiface)

Group Type: OTHER

Associated product 1 : RV2666C

Intervention Type: OTHER

Applied twice a day minimum during 7 days (from Day 1 to Day 7)

Associated product 2 MORNING : RV5000A

Intervention Type: OTHER

Applied in the mornings from Day 8 to Day 95 or Day 176*

• for subjects post injections

Associated product 2 EVENING: RV5000A

Intervention Type: OTHER

Applied in the evenings from Day 8 to Day 95 or Day 176*

• for subjects post injections

Interventions

Associated product 1 : RV2666C

Applied twice a day minimum during 7 days (from Day 1 to Day 7)

Intervention Type: OTHER

Associated product 2 MORNING : RV5000A

Applied in the mornings from Day 8 to Day 95 or Day 176*

• for subjects post injections

Intervention Type: OTHER

Test product : RV4983A

Applied 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

Intervention Type: OTHER

Associated product 2 EVENING: RV5000A

Applied in the evenings from Day 8 to Day 95 or Day 176*

• for subjects post injections

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

Criteria related to the population:

• female and male
• aged between 35 and 70 years included
• phototype: I to IV
• all skin types
• subjects must be registered with health social security or health social insurance
• having signed their written Informed Consent form (ICF) for their participation in the study and a photograph authorization
• certifying the truth of the personal information declared to the Investigator able to understand the language used in the investigation centre and the information given
• able to comply with the protocol and follow protocol's constraints and specific requirements
• cooperative subject, aware of the necessity and duration of controls so that perfect adhesion to the protocol established by the clinical trial centre could be expected (able to comply with the protocol and follow protocol's constraints and specific requirements)
• a maximum of 20% of subjects being lens wearers will be included in the study

Criteria related to the skin condition:

• Subjects having performed superficial rejuvenation procedures on the face including the crow's foot area:

• 20 subjects after peeling (30 or 50% glycolic acid);
• 20 subjects after laser CO2
• 20 subjects after injections of hyaluronic acid or mix containing hyaluronic acid All procedures must remain superficial and aiming an anti-aging effect. Instrumental technics will be on the crow's foot so all procedures must be performed on the face including on this area.

Criteria related to subject's health:

• Considered "healthy subject" by the Investigator
• Women of childbearing potential committing themselves to use effective contraceptive method throughout the study and for at least 3 months before the inclusion visit (with no change during this period)

Criteria related to the population:

• having participated in another clinical trial within the week before the inclusion visit and for a longer period if required in the Investigator's opinion
• taking part or planning to participate in another clinical trial during the study in the same or another investigation centre
• breastfeeding, pregnant (for the women of childbearing potential)
• deprived of freedom by administrative or legal decision or under guardianship - not able to be contacted in case of emergency
• admitted in a sanitary or social facilities
• planning an hospitalization during the study
• belonging to the staff of the investigation centre

Criteria related to the skin condition

• having a dermatological condition liable to interfere with the study data or considered by the Investigator hazardous for the subject or incompatible with the study requirements
• having personal medical history liable to interfere with the study data for the subject or incompatible with the study requirements (except if this population is required by the Sponsor i.e atopic dermatitis)
• having history of abnormal reactions from exposure to sunlight
• having history of hypersensitivity or intolerance to any cosmetic product

Criteria related to treatments

• Topical or systemic treatment liable to interfere with the study data according to investigator's assessment
• having used a self-tanning product during the previous month
• having received, on the study areas, artificial UV exposure or excessive exposure to natural sunlight within the month before the inclusion visit (at Investigator's opinion)

Criteria related to investigational product application areas:

• having had any surgery, chemical or significant invasive dermo-treatment on the experimental area considered by the Investigator liable to interfere with the study data, before the inclusion visit or foreseeing it for the duration of the study (except if the treatment is required by the Sponsor)
• having applied a skincare or make up product on the study areas the day of the inclusion visit (except the usual cleanser)
• having received, on the study areas, artificial UV exposure or excessive exposure to natural sunlight within the 2 weeks before the inclusion visit

Criteria related to the COVID-19:

• subject who does not meet the Ministry of Health guidelines for Covid-19 at the time of the visit

• Minimum Eligible Age: 35 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Pierre Fabre Dermo Cosmetique

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Dermscan Poland

Gdansk, Poland, Poland

Countries

Poland

Other Identifiers

RV4983A20230413

Identifier Type: -

Identifier Source: org_study_id