drugset / Trial / NCT05167864

Evaluation of Four Injectable Neuromodulators in the Glabella Area Glabella Area

NCT05167864

Completed 143 enrolled University of Pennsylvania
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to use 3D imaging to evaluate the effects of four FDA approved neuromodulators on facial lines, wrinkles and animation. Participation is available to women who have never had a cosmetic procedure above the malar region nor a treatment with a neuromodulator within 12 months. All subjects will undergo 3D imaging using the VECTRA M3 (Canfield Scientific, Inc, Fairfield, NJ) prior to treatment with a neuromodulator in order to determine their baseline dimensions. Imaging will be repeated post injection to determine change over time.

Timeline

Start
2022-03-04
Primary completion
2023-06-30
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Botulinum toxin type A Protein / enzyme biologic 20 iu
Comparator Botulinum toxin type A Protein / enzyme biologic 60 iu
Comparator PrabotulinumtoxinA Protein / enzyme biologic 20 iu

Indications

No indication recorded.