drugset / Trial / NCT05167864
Evaluation of Four Injectable Neuromodulators in the Glabella Area Glabella Area
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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.