Chin Augmentation and Correction
Conditions
Brief summary
Randomized, evaluator-blinded, no treatment controlled multicenter study to evaluate safety and effectiveness of GP0109 for augmentation and correction or retrusion in the chin region in Canada
Interventions
Injectable gel. Chin correction and augmentation for retrusion
Sponsors
Study design
Eligibility
Inclusion criteria
* subject willing to comply with the requirements of the study * subject intent to receive treatment for augmentation and correction of retrusion in the chin region * subject with mild or moderate (grade 1 or 2) on the GCRS
Exclusion criteria
* subjects presenting with know allergy to HA (hyaluronic acid) filler or amide local anesthetics * subjects with any previous facial surgery below the nasal line or previous HA filler or collagen below the nasal line within 12 months * subjects in any other interventional clinical study within 30 days before baseline
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Responder rate based on the Galderma Chin Retrusion Scale as assessed live by the Blinded Evaluator | 3 months after baseline |
Countries
Canada