Status:
UNKNOWN
Efficacy of Sumatriptan With Naprosyn in Migraine With Aura
Lead Sponsor:
Dent Neurologic Institute
Conditions:
Migraine With Aura
Eligibility:
All Genders
18-50 years
Phase:
NA
Brief Summary
This is a double-blinded placebo study, examining the efficacy of Sumatriptan with Naprosyn in the treatment of migraine with aura.
Eligibility Criteria
Inclusion
- Subjects must be 18 to 50 years of age, inclusive.
- Patients will meet the International Headache Society (IHS) classification criteria for migraine with aura.
- Subjects must carry the diagnosis of 1-2 migraine with aura per month for at least three months before study inclusion. and migraine with aura were included in the study
- Subjects must have an onset of a visual aura that occurs 15-30 minutes before a migraine headache.
- Subjects must be able to understand and complete a migraine diary.
- Subjects must be able to distinguish a migraine with aura from other types of headache.
- Subjects must be in generally good health as confirmed by medical and medication history, baseline physical and neurological exam and vital signs.
- Female subjects must be either a) postmenopausal for one year, b)surgically sterile, c) practicing acceptable birth control for at least one month prior to screening and throughout study, or d) practicing abstinence and agree to continue same throughout study.
Exclusion
- Subjects who have a significant systemic disease other than migraine that is equally painful or more painful.
- Subjects who have other progressive neurological disorders.
- Subjects who have more than 8 migraines or 15 headache days per month.
- Subjects who have previously taken Treximet and failed due to lack of efficacy or adverse side effects.
- Subjects who carry the diagnosis of chronic tension type headache or cluster headache based on the International Headache Society criteria.
- Subject should not have received any other investigative drug within 3 months prior to enrollment in the study.
- Subject who have the diagnosis of seizure disorder, chronic daily headache, uncontrolled hypertension, cardiovascular disease, history of stroke, basilar or hemiplegic migraine, hepatic disease, or active peptic ulcer disease.
- Subjects currently taking or in 3 months prior to study, use of prophylactic migraine medications.
- Subjects who have a known allergy to Sumatriptan or Naprosyn.
- Subjects who in the opinion of Dr. Mechtler have a condition for which they should not be enrolled in the study.
Key Trial Info
Start Date :
October 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2015
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00893594
Start Date
October 1 2010
End Date
December 1 2015
Last Update
February 19 2015
Active Locations (1)
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1
Dent Neurologic Institute
Amherst, New York, United States, 14226