Open Label Study to Assess Long-term Safety of Repeat Administration of Botulinum Toxin Type A for Moderate to Severe Crow's Feet Lines
NCT ID: NCT01818076
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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TERMINATED
PHASE3
311 participants
INTERVENTIONAL
2013-02-28
2013-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Dose A
Dose A: Botulinum toxin type A
Botulinum Toxin Type A
Botulinum toxin type A, Dose A applied to the lateral canthal area
Interventions
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Botulinum Toxin Type A
Botulinum toxin type A, Dose A applied to the lateral canthal area
Eligibility Criteria
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Inclusion Criteria
* Female or male, 18 years of age and above and in good general health
* Women of childbearing potential 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 3 months
* Chemical peel during the 9 months prior to treatment
* Use of prescription retinoid products during the 3 months prior to treatment
18 Years
ALL
No
Sponsors
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Revance Therapeutics, Inc.
INDUSTRY
Responsible Party
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Locations
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Nashville Centre for Laser and Facial Surgery
Nashville, Tennessee, United States
Countries
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Other Identifiers
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RT001-CL023
Identifier Type: -
Identifier Source: org_study_id
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