DaxibotulinimtoxinA for Treatment of Platysmal Neck Bands

Completed · Phase 4

Conditions studied: Aging

In brief

This study seeks to evaluate the effectiveness and duration of action of DaxibotulinumtoxinA for neck rejuvenation through treatment of platysmal bands. This study will consist of one treatment visit with subjects being randomized to receiving 15 or 20 units of DaxibotulinumtoxinA per platysmal band. Subjects will return for 5 follow-up visits at 8, 12, 16, 20, and 24 weeks for evaluation.

Key facts

Study ID

NCT06225492

Run by

Main Line Center for Laser Surgery

People needed

20

Starts

2024-01-01

Expected to finish

2025-01-01

Last updated by the study team

2025-03-19

Who can join

Age: 31 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• >30 years old
• Rating of 2, 3, or 4 on 5-point Merz Neck Scale
• No use of any botulinum toxin in the neck for the past 6 months

You may not qualify if…

• Pregnancy
• Prior adverse reaction or known hypersensitivity to neuromodulators treatment
• Connective tissue disorder
• Scar in the treatment area
• History of dysphagia and/or neuromuscular disorders (such as but not limited to Amyotrophic Lateral Sclerosis, Multiple sclerosis, Myasthenia Gravis, Lambert-Eaton syndrome, others per PI's discretion)
• Active infection in treatment area
• Active moderate or severe inflammatory disease in treatment area such as atopic dermatitis, psoriasis
• Prior treatment with neuromodulators in treatment area (neck) within the past 6 months

Where it is running

• Main Line Center for Laser Surgery — Ardmore, Pennsylvania, United States

Full record on ClinicalTrials.gov

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