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Safety and Effectiveness of Poly-l-lactic Acid (PLLA) for the Improvement in Appearance of Cellulite

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Galderma

Status

Completed

Conditions

Cellulite

Treatments

Device: Sculptra new dilution

Study type

Interventional

Funder types

Industry

Identifiers

NCT05064761
43CASA2006

Details and patient eligibility

About

This pilot study has been designed to evaluate the safety and effectiveness of PLLA as a single regimen for the improvement in appearance of cellulite after changes in reconstitution procedure.

Full description

Cellulite is a topographic and localized skin condition that is commonly found on the posterolateral thighs, buttocks, and abdomen. It is often identified by a dimpled or orange-peel appearance of the skin's surface. The presence of visible cellulite is associated with histologic changes in the dermis, adipose tissue, and septae.

Based on the theory that a stronger skin structure, with a decrease in skin laxity and increase in dermal thickness, could reduce the appearance of cellulite, the Sponsor intends to investigate the safety and effectiveness of PLLA for the improvement in appearance of cellulite in the posterior thighs.

Enrollment

29 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects with intent to undergo treatment to improve appearance of cellulite in the posterior thighs.

Exclusion criteria

  • Known/previous allergy or hypersensitivity to any of the Sculptra constituents.

  • Known/previous allergy or hypersensitivity to lidocaine and other local anesthetics, e.g. amide-type anesthetics, or topical anesthetics or nerve blocking agents.

  • Previous or present multiple allergies or severe allergies, such as manifested by anaphylaxis or angioedema, or family history of these conditions.

  • Previous treatment/procedure in or near the treatment area:

    1. Previous permanent implant, filler, lifting threads, or autologous fat in the treatment area, regardless of time.
    2. Previous semi-permanent implants exemplified by Calcium Hydroxylapatite (CaHA), poly l-lactic acid (PLLA) in treatment area, regardless of time.
    3. Previous Hyaluronic acid (HA) filler or collagen filler in the treatment area within 12 months.
    4. Previous energy based aesthetic procedures (e.g. laser, intense pulsed light, radiofrequency and endermology) in the treatment area within 6 months.
    5. Previous mechanical (e.g. dermabrasion, needling) or chemical aesthetic procedures (e.g. chemical peel) in the treatment area within 6 months.
    6. Previous treatment with cryotherapy, lipolytic treatments or liporeduction massage in the treatment area within 6 months.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

29 participants in 1 patient group

Treatment group
Experimental group
Description:
PLLA new dilution for treatment to improve appearance of cellulite.
Treatment:
Device: Sculptra new dilution

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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