A Retrospective Study to Evaluate the Effectiveness and Benefit of onabotulinumtoxinA in Patients With Chronic Migraines

NCT ID: NCT01749410

Last Updated: 2015-09-10

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

33 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-05-31

Study Completion Date

2014-05-31

Brief Summary

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This study will evaluate the effectiveness and benefit of treatment with onabotulinumtoxinA in Chronic Migraine patients who have received a minimum of 7 treatment cycles.

Detailed Description

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Conditions

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Chronic Migraine, Headaches

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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All participants

Previous treatment with onabotulinumtoxinA for Chronic Migraine based on retrospective medical record review.

onabotulinumtoxinA

Intervention Type BIOLOGICAL

Previous treatment with onabotulinumtoxinA for Chronic Migraine.

Interventions

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onabotulinumtoxinA

Previous treatment with onabotulinumtoxinA for Chronic Migraine.

Intervention Type BIOLOGICAL

Other Intervention Names

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Botulinum Toxin Type A BOTOX®

Eligibility Criteria

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Inclusion Criteria

* 15 or more headache days over a 30 day period
* A minimum of 7 treatment cycles with onabotulinumtoxinA

Exclusion Criteria

* Any treatment cycle dose of onabotulinumtoxinA greater than 200 units
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 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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Encinitas, California, United States

Site Status

Countries

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United States

Other Identifiers

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GMA-BTX-CM-12-491

Identifier Type: -

Identifier Source: org_study_id

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