NCT Number: NCT00210821
Comparing the Safety and Effectiveness of Topiramate With the Safety and Effectiveness of Amitriptyline in Preventing Migraine Headaches
The purpose of this study is to compare the effectiveness and safety of two treatment regimens in preventing migraines. The antidepressant amitriptyline has been used successfully to prevent migraine headaches.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
About this study
People who suffer from migraines have many prescription medications to choose from, both to treat the migraine and to prevent it from starting. However, many patients have not had success in finding the drug that helps them best. Amitriptyline, an antidepressant, has been used successfully for many years to prevent migraine headaches. This study will compare the effectiveness of amitriptyline with the effectiveness of topiramate, an anti-seizure drug, in preventing migraines. The safety of both drugs will also be assessed. The objective of the study is to demonstrate that topiramate will be at least as effective as amitriptyline in preventing migraines. During the first 4 weeks of the study, topiramate or amitriptyline will be increased by 25 mg per week up to a total dose of 100 mg per day or up to the maximum tolerated dose, whichever is less. Treatment will continue at 100 mg per day for 22 weeks.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Migraine headache for at least 6 months, with 3 to 12 headaches a month for the previous 3 months
- no more than 15 headache days in the previous month before study start
- no heart rhythm problems or neurologic problems
- women must not be pregnant and must use birth control
Exclusion criteria
- Cannot have failed at least 2 previous trials of migraine prevention drugs
- cannot have failed a previous trial of topiramate or amitriptyline
- no cluster headaches
- no migraine with aura without headache
- no pain that is worse than the migraine pain
Treatment and study plan
Primary outcomes
-
Change from baseline in the average monthly migraine episode rate.
Secondary outcomes
-
Change in average monthly rate of days with migraine headache; change in average monthly rate of headache (migraine & non-migraine) days; change in average monthly rate of acute abortive medications; weight changes; quality of life assessments
Sponsors and collaborators
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Industry
Collaborators
- Ortho-McNeil Neurologics, Inc.
Registry information
Official study title
A Comparison of Topiramate Versus Amitriptyline in Migraine Prophylaxis
Important dates
- Study start
- 2004
- Study completion
- 2005
- First posted
- Sep 21, 2005
- Registry last updated
- Jun 10, 2011
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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