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NCT05691972

Effectiveness and Safety of Restylane Contour in the Treatment of Temple Hollowing

Completed NA Last updated 17 February 2025
What this trial tests

NA trial testing Restylane Contour in Temporal Hollowing in 225 participants. Completed in 11 December 2024.

Timeline
14 March 2023
Primary endpoint
26 October 2023
11 December 2024

Quick facts

Lead sponsorGalderma R&D
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment225
Start date14 March 2023
Primary completion26 October 2023
Estimated completion11 December 2024
Sites15 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Galderma R&D — full company profile →

Who can join

22 and older, any sex, with Temporal Hollowing. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a randomized, no-treatment-controlled, evaluator-blinded, multi-center study to evaluate the effectiveness and safety of Restylane® Contour in correction of temple hollowing.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Restylane Contour

Trials testing the same drug.

Other Galderma R&D 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/NCT05691972.

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