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Clinical Trials/NCT03606356
NCT03606356
Completed
Phase 4

Sustained onabotulinumtoxinA Therapeutic Benefits in Patients With Chronic Migraine Over 3 Years of Treatment. A

Corfu Headache Clinic0 sites56 target enrollmentApril 1, 2015

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Migraine Disorders
Sponsor
Corfu Headache Clinic
Enrollment
56
Primary Endpoint
Change in the mean number of monthly headaches
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

To assess whether there is a sustained benefit and good safety with repeated onabotulinumtoxinA sessions in chronic migraine over more than three years of treatment.

We prospectively enrolled 65 chronic migraine patients, who were classified as responders after three sessions of onabotulinumtoxin A and were eligible to further continue treatment.

Detailed Description

Evidence on whether the therapeutic effect and good safety profile of onabotulinumtoxinA (Botox®) in chronic migraine (CM) patients is maintained over long term treatment is still limited. This study aims at assessing whether there is a sustained benefit and good safety with repeated onabotulinumtoxin A sessions in CM over more than three years of treatment. This study prospectively enrolled 65 CM patients, who were classified as responders after three sessions of onabotulinumtoxinA and were eligible to further continue treatment. Data documenting longitudinal changes from the trimester after the third onabotulinumtoxinA administration (T1) to the trimester after completing two years of treatment (T2) and eventually to the trimester after completing three years of treatment (T3) in (i) mean number of monthly headache days (ii) migraine severity as expressed by the mean number of days with peak headache intensity of \>4/10, and (iii) mean number of days with use of any acute headache medication, were prospectively collected from patients' headache diaries.

Registry
clinicaltrials.gov
Start Date
April 1, 2015
End Date
April 1, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Corfu Headache Clinic
Responsible Party
Principal Investigator
Principal Investigator

KONSTANTINOS SPINGOS

Konstantinos Spingos MD, Neurologist

Corfu Headache Clinic

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with chronic migraine according to IHC-III with or without medication overuse.
  • Responders defined as patients that after 3 sessions of treatment with onabutulinum toxin A, having experienced a ≥50% reduction in their average monthly migraine days

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in the mean number of monthly headaches

Time Frame: 3 years

Change in the mean number of monthly headache days, from the third administration (months 10 to 12; T1) to the period after three years of treatment (months 37-39; T3)

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