Overview

Efficacy of Zolmitriptan (Zomig) in the Treatment of Migraines in Adolescents

Status:
Completed
Trial end date:
2004-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to evaluate the effectiveness and safety of Zolmitriptan (Zomig) nasal spray, 5.0 mg, compared with placebo (inactive drug) for 2 migraine headaches over a 3-month period in adolescent patients (aged 12 to 17 years) with migraine headaches
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AstraZeneca
Treatments:
Oxazolidinones
Zolmitriptan
Criteria
Inclusion Criteria:

- Adolescents aged 12-17 years at the time of screening. Patients must not be enrolled
if they will turn 18 years of age within 12 weeks after randomization.

- An established diagnosis of migraine for at least 1 year; a minimum of 2 migraines,
considered to be moderately/severely disabling, per month on average during the school
year

- A history of usual migraine duration of >2-hours untreated for the 3 month prior to
screening

Exclusion Criteria:

- A history of basilar, ophthalmoplegic or hemiplegic migraine headache or any
potentially serious neurological condition that is associated with headache or
clinically significant abnormalities indicated from the medical history, physical exam
etc

- Has used monoamine oxidase inhibitor-A (MAO-A), methysergide, methylergonovine or
cimetidine in the 2 weeks before randomization.

- Evidence of ischemic heart disease, arrhythmia, accessory conduction pathway disorder
as determined by central cardiologist using predetermined and agreed upon pediatric
standards; Has uncontrolled hypertension