Safety and Effectiveness of BOTOX® for Lateral Canthal Lines With or Without Simultaneous Glabellar Lines in Korea

NCT ID: NCT02248844

Last Updated: 2019-07-05

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

667 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-09-26

Study Completion Date

2017-08-14

Brief Summary

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This is a postmarketing surveillance study in Korea to evaluate the safety and effectiveness of BOTOX® for lateral canthal lines (crow's feet lines) with or without simultaneous glabellar lines.

Detailed Description

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Conditions

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Lateral Canthal Lines Crow's Feet Lines

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Botulinum Toxin Type A

Subjects who receive botulinum toxin Type A injected into crow's feet line areas per clinical practice.

Botulinum Toxin Type A

Intervention Type BIOLOGICAL

Botulinum toxin Type A injected into crow's feet line areas per clinical practice.

Interventions

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Botulinum Toxin Type A

Botulinum toxin Type A injected into crow's feet line areas per clinical practice.

Intervention Type BIOLOGICAL

Other Intervention Names

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BOTOX® onabotulinumtoxinA

Eligibility Criteria

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Inclusion Criteria

* Subject and Investigator decision to treat crow's feet lines with Botox®

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Allergan

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Director

Role: STUDY_DIRECTOR

Allergan

Locations

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Dr. Robbin Clinic

Gangnam-gu, Seoul, South Korea

Site Status

Countries

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South Korea

Related Links

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Other Identifiers

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191622-147

Identifier Type: -

Identifier Source: org_study_id

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