Status:
COMPLETED
Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's Feet Lines
Lead Sponsor:
Allergan
Conditions:
Lateral Canthus Rhytides
Crow's Feet Lines
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
This study will evaluate the safety and efficacy of botulinum toxin Type A compared to placebo for the treatment of Crow's Feet Lines (Lateral Canthal Rhytides).
Eligibility Criteria
Inclusion
- Moderate to severe Crow's Feet Lines
- Have adequate vision without the use of eyeglasses to assess facial wrinkles in a mirror (contact lenses OK)
Exclusion
- Current or previous botulinum toxin treatment of any serotype
- Facial laser or light treatment, microdermabrasion or superficial peels within 3 months
- Oral retinoid therapy within 1 year
- Prior facial cosmetic surgery (eg, periorbital surgery, facial lift, brow lift, eye lift, or eyebrow surgery)
- Diagnosis of myasthenia gravis, Eaton-Lambert syndrome, amyotrophic lateral sclerosis
Key Trial Info
Start Date :
October 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2011
Estimated Enrollment :
446 Patients enrolled
Trial Details
Trial ID
NCT01189747
Start Date
October 1 2010
End Date
July 1 2011
Last Update
May 7 2019
Active Locations (4)
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1
Newport Beach, California, United States
2
Aalst, Belgium
3
Vancouver, British Columbia, Canada
4
Sutton Coldfield, England, United Kingdom