Efficacy and Safety Study of Botulinum Toxin Type A for Moderate to Severe Crow's Feet Lines
NCT ID: NCT01776606
Last Updated: 2014-05-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
247 participants
INTERVENTIONAL
2012-12-31
2013-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Dose A
Dose A: Botulinum toxin type A
Botulinum Toxin Type A
Botulinum Toxin Type A, Dose A; dose applied to the lateral canthal lines
Dose B
Dose B: Placebo
Placebo
Placebo, Dose B; dose applied to the lateral canthal lines
Interventions
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Botulinum Toxin Type A
Botulinum Toxin Type A, Dose A; dose applied to the lateral canthal lines
Placebo
Placebo, Dose B; dose applied to the lateral canthal lines
Eligibility Criteria
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Inclusion Criteria
* Female or male, 18 to 65 years of age and in good general health
* Women of childbearing potential (WOCBP) must agree to use an effective method of birth control during the course of the study
Exclusion Criteria
* Muscle weakness or paralysis, particularly in the area receiving study treatment
* Active skin disease or irritation at the treatment area
* Deep dermal scarring, or inability to smooth out the crow's feet lines to be treated by manually spreading the skin apart
* Treatment with botulinum toxin type A for crow's feet lines in the last 6 months
18 Years
65 Years
ALL
No
Sponsors
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Revance Therapeutics, Inc.
INDUSTRY
Responsible Party
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Locations
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Dermatology Research Institute
Coral Gables, Florida, United States
Countries
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Other Identifiers
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RT001-CL019
Identifier Type: -
Identifier Source: org_study_id
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