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Evaluating Facial Skin Quality Changes Post-Lipofilling

A MONOCENTER, OPEN STUDY TO ASSESS THE CHANGES INDUCED BY A LIPOFILLING PROCEDURE ON FACIAL SKIN QUALITY AND AGEING SIGNS IN WOMEN

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07737639
Enrollment
15
Registered
2026-07-30
Start date
2021-01-10
Completion date
2024-09-10
Last updated
2026-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Facial Aging

Keywords

autologous fat grafting, lipofilling, facial rejuvenation, adipose-derived stem cells, skin quality

Brief summary

The goal of this prospective observational study is to evaluate changes in facial skin quality and identify predictive biological markers in donor adipose tissue in healthy women undergoing autologous facial fat transfer. The main questions it aims to answer are: How does full-face lipofilling alter clinical signs of aging, such as wrinkles, sagging, and skin texture, over a 6-month period? Which baseline biological characteristics (e.g., cellular stemness, extracellular matrix remodeling, angiogenesis) within the donor fat graft predict these clinical skin quality outcomes? Participants will: Undergo a standard full-face autologous fat transfer (lipofilling) procedure. Attend follow-up evaluation visits at 1.5, 3, and 6 months post-procedure. Undergo non-invasive clinical and instrumental skin assessments (e.g., standardized photography, 3D topography, echography, and cutometry). Complete self-assessment questionnaires regarding perceived skin changes and overall satisfaction with the procedure.

Interventions

None listed

Sponsors

L'Oreal
Lead SponsorINDUSTRY
Hospices Civils de Lyon
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
30 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Female patient volunteers 2. Over the age of 30 3. Who had decided to have adipose tissue injections and declared eligible to this intervention 4. Nonsmoker or less than 5 cigarettes per day 5. Informed about the study objectives and procedures, and able to understand them 6. Willing and able to fulfil the study requirements and schedule 7. Able to give their written informed consent 8. French subjects recruited must be affiliated to the French social security system.

Exclusion criteria

1. Having participated within the 30 days before inclusion or currently participating in another clinical study. 2. Females in pregnancy or nursing 3. Dermatological disorder affecting the investigational areas (like severe acne, rosacea eczema, atopy, psoriasis, seborrheic dermatitis) that may interfere with the study conduct or the study results in the opinion of the Investigator, 4. History of skin cancer or auto-immune disease, 5. History of allergy, hypersensitivity, or any serious reaction to any medicinal or cosmetic product, 6. Any concomitant medical condition that may interfere with the study conduct in the opinion of the investigator (diabetes, HIV+, hepatitis B and C…) 7. Surgical procedure to the face (face lift) 8. Cosmetic procedures: filler injection, botulinum toxin injection, laser to the face within the past 4 months 9. Actual or past use of systemic or topic drugs, that would interfere with assessment and/or investigational treatments and affect study results in the opinion of the investigator

Design outcomes

Primary

MeasureTime frameDescription
Change in Wrinkles and Fine Lines SeverityBaseline up to 6 months post-procedureAssessed by a trained expert using dynamic scales and photonumeric atlas books. This category evaluates the severity of crow's feet (grade 0-6), underneath eye wrinkles (grade 0-5), forehead wrinkles (grade 0-5), upper lip wrinkles (grade 0-6), nasolabial folds (grade 0-5), and cheek folds (grade 0-8). For all scales, a lower grade indicates less severe wrinkles (clinical improvement).
Change in Skin Pigmentation and Color UniformityBaseline up to 6 months post-procedureThis category includes assessments of lateral and malar pigmentation (6-point scale), dark circles (grade 0-8), full face dyschromia/skin tone heterogeneity (6-point scale), and cheek erythrosis/redness (6-point scale). Lower grades indicate reduced pigmentation and more uniform skin tone (clinical improvement).
Change in Skin Elasticity, Sagging, and Structural Aging SignsBaseline up to 6 months post-procedureAssessed clinically and via standardized photographs to evaluate structural skin changes. This includes grading of sagging/lower facial ptosis (grade 0-5), eye bags (grade 0-7), clinical skin elasticity on the cheek (6-point scale), and full face elastosis (6-point scale). Lower grades indicate less sagging and elastosis (clinical improvement).
Change in Skin Texture and Surface QualityBaseline up to 6 months post-procedureThis comprehensive category encompasses full face brightness (6-point scale, where higher is better), pore visibility (grade 0-7), water mobility (grade 0-10), papyraceus/papery aspect of the cheek (6-point scale), and skin surface parameters including oiliness, shininess, dryness, and roughness (4-point scales). With the exception of brightness, lower grades generally indicate smoother, improved skin texture.

Countries

France

Contacts

STUDY_DIRECTORStephanie Nouveau

L'Oreal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026