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New Dermal Filler for Chin Correction and Augmentation

A Randomized, Evaluator-blinded, Parallel Group, no Treatment Controlled, Multi-center Study to Evaluate Effectiveness and Safety of GP0109 for Augmentation and Correction of Retrusion in the Chin Region

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04631263
Enrollment
140
Registered
2020-11-17
Start date
2021-01-29
Completion date
2022-06-16
Last updated
2022-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chin Augmentation and Correction

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

DEVICEHyaluronic Acid

Injectable gel. Chin correction and augmentation for retrusion

Sponsors

Galderma R&D
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes

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

MeasureTime frame
Responder rate based on the Galderma Chin Retrusion Scale as assessed live by the Blinded Evaluator3 months after baseline

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026