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NCT05445661

Sculptra to Aid in Treatment of Arm Laxity

Status unknown NA Last updated 6 July 2022
What this trial tests

NA trial testing injectable poly-L-lactic acid in Skin Laxity in 20 participants. Status unknown.

Timeline
20 July 2022
Primary endpoint
20 September 2023
20 September 2023

Quick facts

Lead sponsorGoldman, Butterwick, Fitzpatrick and Groff
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment20
Start date20 July 2022
Primary completion20 September 2023
Estimated completion20 September 2023

Drugs / interventions tested

Conditions studied

Sponsor

Goldman, Butterwick, Fitzpatrick and Groff — full company profile →

Who can join

Adults 40 to 70, female only, with Skin Laxity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To assess the safety, efficacy, and patient satisfaction associated with the treatment of upper inner arm crepiness/laxity with injectable poly-L-lactic acid (PLLA, Sculptra® Aesthetic; Galderma Laboratories; Fort Worth, TX).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Injectable Poly-L-Lactic Acid for Body Aesthetic Treatments: An International Consensus on Evidence Assessment and Practical Recommendations.
    Haddad A, Avelar L, Fabi SG, Sarubi J, et al · · 2025 · cited 4× · PMID 39592491 · DOI 10.1007/s00266-024-04499-9

Verify or expand the search:

Other trials of injectable poly-L-lactic acid

Trials testing the same drug.

Other recruiting trials for Skin Laxity

Currently open trials in the same condition.

Other Goldman, Butterwick, Fitzpatrick and Groff trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05445661.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing