Recruiting
A Study to Characterize Human Skin Changes From Biostimulator Treatments Via Non-invasive Imaging
Galderma R&D · NCT07399028
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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 45–65 · Women only
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 25
- US sites recruiting
- 1
- Study start
- October 21, 2025
- Record last updated
- February 10, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Adult subjects with moderate-to-severe cheek wrinkles will be treated with Sculptra for correction of fine lines and wrinkles in the cheek area.
Being studied: Sculptra®
Conditions: Volume Deficiency in the Mid-Face; Skin Laxity; Photo-aged Skin
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Adult subjects aged 45-65 years old
- Females only
- Subject with moderate-to-severe cheek wrinkles on the GCWS
- Subject with intent to undergo correction of cheek wrinkles on both sides of the face
- Subject who in the opinion of the Investigator would need 3 treatments for optimal clinical outcomes
- Subject willing to be photographed at each visit.
- Subjects willing to stop using current facial skincare products for the duration of the study.
- Subject willing to replace the current facial skincare products with the provided facial skincare products, including cleanser, moisturizer and sunscreen, until study completion.
- Ability to read, understand and give consent for participation in the study.
- Agreement to adhere to the procedures and requirements of the study and to report to the site on the day(s) and at the time(s) scheduled for the assessments.
Exclusion Criteria
- Subjects with a history of allergy or hypersensitivity to any ingredient of the treatment products.
- Previous tissue-augmenting therapy, contouring, or revitalization treatment in the face, except lips.
- Previous treatment/procedure in the face in the previous 6 months that, in the Investigator's opinion, would interfere with the study injections and/or study assessments or exposed the study subject to undue risk by study participation, or planning to undergo any of these procedures affecting the treatment area at any time during the study.
- Subjects with any medical condition that, in the opinion of the Investigator, would make the subject unsuitable for inclusion.
Recruiting US locations
Luxurgery
New York, NY 10021
Site contact: Christina Uong · 212-508-0000 · cku@luxurgery.com