CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,168 enrolled
Drug / intervention
botulinum toxin Type Abiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01432379
NCT01432379N/ACompleted

BOTOX® Prophylaxis in Patients With Chronic Migraine

Allergan·observational·Posted Sep 13, 2011·Updated Jan 8, 2019

In Brief

An observational study evaluating botulinum toxin Type A for Migraine Disorders. Completed, enrolled 1,168 participants across 4 sites in 4 countries.

Detailed Summary

This is a post authorization observational study to monitor the utilization practices and describe the safety profile of BOTOX® in clinical practice for the prophylactic treatment of headaches in adult patients with chronic migraine.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGermany, Spain, Sweden, United Kingdom
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedSep 13, 2011
Enrollment StartSep 9, 2011
Primary CompletionMay 12, 2015
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 14.8 years ago

Interventions

botulinum toxin Type Abiological

155-195 U of botulinum toxin Type A administered intramuscularly in the face, head, and neck areas as directed by physician (approximately every 12 weeks) for 1 year.