Migraine | The Childhood and Adolescent Migraine Prevention Study
Migraine research study
What is the primary objective of this study?
The purpose of this research study is to test two medicines for migraine prevention in children and adolescents.
Who is eligible to participate?
Inclusion Criteria: - Migraine with or without aura (International Classification of Headache Disorders, 2nd Edition (ICHD-II) or chronic migraine (ICHD-II revised) - Migraine frequency based upon prospective headache diary of 28 days must be ≥ 4. Migraine frequency defined as any migraine during one day in the 28 day baseline period (1) - PedMIDAS Disability Score > 10, indicating at least mild disruption in daily activities and < 140, indicating extreme disability that may require more comprehensive, multi-component therapy - Females or males 8-17 years, inclusive 1. Migraine frequency is defined as the period from the onset to the stop time of painful migraine symptoms not to exceed 24 hours with the clock starting at midnight. If painful symptoms last longer than 24 hours, this is considered a new and distinct migraine headache. If painful symptoms recur within 24 hours of initial onset, this is considered part of the initial migraine episode and would be counted as one migraine. Exclusion Criteria: - Continuous migraine defined as an unrelenting headache for a 28 day period - Weight less than 30 kg or greater than 120 kg - Unwilling to avoid taking non-specific acute medication such as NSAIDS (e.g., ibuprofen), more than 3 times per week, or migraine specific acute medications such as triptans more than 6 times per month - Currently taking other prophylactic anti-migraine medication within a period equivalent to 2 weeks of that medication before entering the screening phase, or the use of Botulinum toxin (Botox®) within 3 months of entering the screening phase - Subjects who have previously failed an adequate trial of AMI or TPM for prophylaxis of at least 3 months duration at doses recommended for migraine relief because of lack of efficacy or adverse events(2) - Current use of disallowed medications/products: opioids, antipsychotics, antimanics, barbiturates, benzodiazepines, muscle relaxants, sedatives, tramadol, nutraceuticals, SSRIs, or SSNRIs - Known history of allergic reaction or anaphylaxis to AMI or TPM - Abnormal findings on ECG at baseline, particularly lengthening of the QT interval greater than or equal to 450 msec - Subject is pregnant or has a positive pregnancy test - Subject is sexually active and not using a medically acceptable form of contraception - Diagnosis of epilepsy or other neurological diseases - History of kidney stones - Inability to swallow pills after using behavioral techniques if indicated between screening visit and baseline visit (3) - Present psychiatric disease as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM IV) (e.g. psychosis, bipolar disorder, major depression, generalized anxiety disorder), alcohol or drug dependence, or documented developmental delays or impairments (e.g., autism, cerebral palsy, or mental retardation) that, in the opinion of the site investigator, would interfere with adherence to study requirements or safe participation in the trial - Any and all other diagnoses or conditions which in the opinion of the site investigator, that would prevent the patient from being a suitable candidate for the study or interfere with the medical care needs of the study subject (2)\"Previously failed an adequate trial of AMI or TPM\" is defined as: dosage of 1mg/kg/day of AMI or 2 mg/kg/day of TPM; trial of at least 3 months duration; efficacy of having at least a 50% decrease in migraine frequency in response to drug therapy; or unable to tolerate taking the medication due to treatment-related side effects. (3)Subjects who cannot swallow pills at the time of the screening visit will be given a training session using behavioral techniques. Upon return for baseline visit, if the subject continues to be unable to swallow pills, the subject will be excluded from the study.
Which medical condition, disease, disorder, syndrome, illness, or injury is researched?
Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.
Drug:AmitriptylineAmitriptyline will be administered twice daily at home during the 8-week titration period followed by a 16 week maintenance phase of the highest tolerated dose. The morning dose is a placebo pill. Dosing of amitriptyline will be weight-based.
Drug:TopiramateTopiramate will be administered twice daily at home during the 8-week titration period followed by a 16 week maintenance phase of the highest tolerated dose. Dosing of topiramate will be weight-based.
Drug:PlaceboPlacebo will be administered twice daily at home during the 8-week titration period followed by a 16 week maintenance period.
Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.
AmitriptylineDrug to be administered twice daily.
TopiramateDrug to be administered twice daily.
PlaceboTo be administered twice daily.
Start Date: June 2012
Completed Date: January 2016
Phase: Phase 3
Primary Outcome: Number (Percentage) of Participants Reporting a ≥ 50% Reduction in Headache Days
Secondary Outcome: Change in Absolute Headache Disability Score on PedMIDAS
Study sponsors, principal investigator, and references
Principal Investigator: Scott W. Powers, PhD
Lead Sponsor: Children's Hospital Medical Center, Cincinnati
Collaborator: National Institute of Neurological Disorders and Stroke (NINDS)