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New Dermal Filler for Chin Correction and Augmentation

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Galderma

Status

Completed

Conditions

Chin Augmentation and Correction

Treatments

Device: Hyaluronic Acid

Study type

Interventional

Funder types

Industry

Identifiers

NCT04631263
43BBJ2001

Details and patient eligibility

About

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

Enrollment

140 patients

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

140 participants in 2 patient groups

Treatment Group
Experimental group
Treatment:
Device: Hyaluronic Acid
Control Group
No Intervention group

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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