Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat Chronic Migraine in Korea

NCT ID: NCT01976611

Last Updated: 2015-04-08

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

402 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-06-30

Study Completion Date

2015-02-28

Brief Summary

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This study is a Post-Marketing Surveillance study in Korea to evaluate the safety and efficacy of botulinum toxin Type A to treat Chronic Migraine in clinical practice.

Detailed Description

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Conditions

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Migraine Disorders Headache

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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BOTOX®

Patients who receive botulinum toxin Type A (BOTOX®) treatment for chronic migraine as per local standard of care in clinical practice.

botulinum toxin Type A

Intervention Type BIOLOGICAL

Botulinum toxin Type A treatment for chronic migraine as per local standard of care in clinical practice.

Interventions

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botulinum toxin Type A

Botulinum toxin Type A treatment for chronic migraine as per local standard of care in clinical practice.

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Patients treated with botulinum toxin Type A for chronic migraine in clinical practice.

Exclusion Criteria

* None.
Minimum Eligible Age

18 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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Seoul, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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191622-139

Identifier Type: -

Identifier Source: org_study_id

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