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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00632385
Other study ID # A1601092
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date January 2003
Est. completion date August 2003

Study information

Verified date January 2021
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess the efficacy and safety of eletriptan for migraine headaches in subjects who were not satisfied with rizatriptan therapy


Recruitment information / eligibility

Status Completed
Enrollment 127
Est. completion date August 2003
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Diagnosis of migraine headache according to International Headache Society criteria and migraine headaches for at least 1 year - Eletriptan naive - Previously treated with rizatriptan and failed to achieve a satisfactory response within the past 12 months Exclusion Criteria: - Non-migraine headaches on average more than 6 days per month or have less than 24 hours of freedom from headache between migraine attacks - Migraine attacks that are atypical or chronic daily headaches - A history of migraine with prolonged aura, familial hemiplegic migraine, basilar migraine, migrainous infarction, migraine aura without headache, migraine with acute onset aura

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Eletriptan
40 mg oral tablet for migraine attack, followed by 40 mg oral tablet if migraine reoccurred >2 hours from first dose and within 24 hours of first dose

Locations

Country Name City State
United States Pfizer Investigational Site Alexandria Virginia
United States Pfizer Investigational Site Chesterfield Missouri
United States Pfizer Investigational Site Cincinnati Ohio
United States Pfizer Investigational Site Eugene Oregon
United States Pfizer Investigational Site Greensboro North Carolina
United States Pfizer Investigational Site Irvine California
United States Pfizer Investigational Site Marietta Georgia
United States Pfizer Investigational Site Milford Massachusetts
United States Pfizer Investigational Site Newport Beach California
United States Pfizer Investigational Site Plantation Florida
United States Pfizer Investigational Site Saint Petersburg Florida
United States Pfizer Investigational Site San Antonio Texas
United States Pfizer Investigational Site San Francisco California
United States Pfizer Investigational Site South Bend Indiana
United States Pfizer Investigational Site Springfield Missouri
United States Pfizer Investigational Site Tampa Florida

Sponsors (1)

Lead Sponsor Collaborator
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in headache pain severity 1, 2, 4, and 24 hours
Secondary Functional impairment 1, 2, 4, and 24 hours
Secondary Work Productivity Questionnaire Week 10
Secondary Time Loss Week 10
Secondary Subject Preference Questionnaire Week 10
Secondary Global Evaluation Week 10
Secondary Subject Satisfaction Scale Week 10
Secondary Associated Symptoms 1, 2, 4, and 24 hours
Secondary Use of Rescue Medication Week 10
Secondary Adverse events Week 10
Secondary Vital signs Week 10
Secondary Physical examination Week 10
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