Restoring Facial Volume After GLP-1 Weight Loss With Radiesse
Sponsor: Kalpna Kay Durairaj, MD, FACS • ClinicalTrials.gov ID: NCT07419854
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The goal of this clinical trial is to evaluate the potential of Calcium Hydroxylapatite (CaHA) to restore facial volume and improve skin quality in patients with GLP-1 receptor agonist-associated facial volume loss. Participants will: * Schedule first dose of a prescribed GLP-1 receptor agonist drug to coincide with the baseline visit of this study * Be randomly assigned to one of two groups (Group A will receive off-label injections of hyperdiluted CaHA at Month 0. Group B will receive on-label injections of CaHA after serving as a control group through Month 6) * Have clinical photos taken at each office visit to track progress
Interventions
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Hyperdiluted Calcium Hydroxylapatite
(Device)
Each syringe of CaHA contains 1.5 cc of product, and it will be diluted 1:2 with 0.5 cc of 1% Lidocaine and 2.5 cc of normal saline.
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Calcium hydroxylapatite
(Device)
Each syringe of CaHA contains 1.5 cc of product, and 0.26 mL of 1% Lidocaine will be added to each syringe. This will be used to target facial folds and wrinkles.
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Calcium hydroxylapatite with integral lidocaine
(Device)
Each syringe contains 1.5 cc of product and will be used as is to target the jawline and body of the mandible.
Eligibility criteria
Conditions
Locations
- K. Kay Durairaj, MD, A Medical Corp. — Pasadena, California, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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