Assess Impact of Poly-L-lactic Acid on GLP1 Subjects
Part of paid clinical trials in San Diego, California.
- Sponsor
- Goldman, Butterwick, Fitzpatrick and Groff
- Study ID
- NCT07217743
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
- Laxity; Skin
Eligibility Criteria
- Sex
- FEMALE
- Age
- 25 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Sculptra Aesthetic — DEVICE15 GLP1 subjects treated with Sculptra to their abdomen for skin laxity will be compared to 5 non GLP1 subjects treated with Sculptra for skin laxity.
Study Details
Clinical trial to evaluate treatments of double-dilute poly-L-lactic acid on abdominal skin laxity in GLP1 patients versus non GLP1 patients.
Key Dates
- Start date
- Oct 27, 2025
- Status verified
- Oct 2025
- Primary completion
- Aug 30, 2026
- Completion
- Oct 31, 2026
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: GLP1 Patients15 Participants who have been on a stable dose of GLP1 for at least 6 months will receive three treatments, one month apart, of Sculptra Aesthetic up to 16cc.
- Experimental: NON GLP1 Patients5 participants who are GLP1 naive will receive three treatments, one month apart, of Sculptra Aesthetic up to 16cc.
Primary Outcome Measure
Physical Global Aesthetic Improvement Scale [ Time Frame: Month 3 and Month 9 ]
Central Contacts
- Andrea Pacheco858-657-1004
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| West Dermatology Research Center | San Diego | California | 92121 |
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