A Safety and Efficacy Study of OnabotulinumtoxinA in Upper Facial Rhytides



Status:Active, not recruiting
Conditions:Cosmetic
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:October 2014
End Date:April 2016

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This is a safety and efficacy study of onabotulinumtoxinA in subjects with upper facial
rhytides (forehead lines, glabellar lines, lateral canthal lines [crow's feet lines]).


Inclusion Criteria:

- Moderate to severe forehead lines, glabellar lines, and crow's feet lines

- Willing to have facial photos taken

Exclusion Criteria:

- Prior exposure to botulinum toxin of any serotype for any indication

- Anticipated need for treatment with botulinum toxin of any serotype for any
indication during the study, other than study treatment

- Diagnosis of myasthenia gravis, Eaton-Lambert syndrome, or amyotrophic lateral
sclerosis

- Any facial resurfacing laser or light treatment, microdermabrasion, or superficial
peels in the past 3 months

- Any medium depth or deep depth facial chemical peels; facial skin resurfacing; or
permanent facial make-up in the past 6 months

- Any nonpermanent soft tissue fillers, or treatment with oral retinoids in the past
year - Prior face lift, thread lift, eyebrow lift, or related procedures (eg, eyelid
and/or eyebrow surgery)

- Prior facial treatment with permanent soft tissue fillers, synthetic implants (eg,
Gore-Tex®), and/or fat transplantation
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