Study to Test a Marketed Drug in the Treatment of Menstrual Migraine (0462-072)
Primary Purpose
Migraine
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
MK0462, rizatriptan benzoate / Duration of Treatment -1day
Comparator: placebo / Duration of Treatment - 1 day
Sponsored by
About this trial
This is an interventional treatment trial for Migraine
Eligibility Criteria
Inclusion Criteria: Female patient at least 18 years old Patient has menses approximately monthly Patient has at least a 6 month history of migraine and at least a 6 month history of menstrual migraine Exclusion Criteria: Pregnant and/or nursing mother Cardiovascular disease Uncontrolled hypertension
Sites / Locations
Outcomes
Primary Outcome Measures
Percentage of patients with 2 hour pain relief: 4-point headache severity scale as recorded in patient diary
Secondary Outcome Measures
Percentage of patients with 24-hr sustained pain relief: headache severity between 2 and 24 hrs post dose recorded in patient diary
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00111722
Brief Title
Study to Test a Marketed Drug in the Treatment of Menstrual Migraine (0462-072)
Official Title
A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo Controlled Study to Evaluate the Efficacy and Tolerability of Rizatriptan 10 mg Tablets for the Treatment of Menstrual Migraine
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
May 27, 2005 (Actual)
Primary Completion Date
February 15, 2006 (Actual)
Study Completion Date
February 23, 2006 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Organon and Co
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to test the effectiveness of a marketed drug in the treatment of a menstrual migraine attack.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
393 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
MK0462, rizatriptan benzoate / Duration of Treatment -1day
Intervention Type
Drug
Intervention Name(s)
Comparator: placebo / Duration of Treatment - 1 day
Primary Outcome Measure Information:
Title
Percentage of patients with 2 hour pain relief: 4-point headache severity scale as recorded in patient diary
Secondary Outcome Measure Information:
Title
Percentage of patients with 24-hr sustained pain relief: headache severity between 2 and 24 hrs post dose recorded in patient diary
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Female patient at least 18 years old
Patient has menses approximately monthly
Patient has at least a 6 month history of migraine and at least a 6 month history of menstrual migraine
Exclusion Criteria:
Pregnant and/or nursing mother
Cardiovascular disease
Uncontrolled hypertension
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Monitor
Organizational Affiliation
Merck Sharp & Dohme LLC
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
17448179
Citation
Mannix LK, Loder E, Nett R, Mueller L, Rodgers A, Hustad CM, Ramsey KE, Skobieranda F. Rizatriptan for the acute treatment of ICHD-II proposed menstrual migraine: two prospective, randomized, placebo-controlled, double-blind studies. Cephalalgia. 2007 May;27(5):414-21. doi: 10.1111/j.1468-2982.2007.01313.x.
Results Reference
background
PubMed Identifier
18422606
Citation
Nett R, Mannix LK, Mueller L, Rodgers A, Hustad CM, Skobieranda F, Ramsey KE. Rizatriptan efficacy in ICHD-II pure menstrual migraine and menstrually related migraine. Headache. 2008 Sep;48(8):1194-201. doi: 10.1111/j.1526-4610.2008.01093.x. Epub 2008 Apr 14.
Results Reference
background
Available IPD and Supporting Information:
Available IPD/Information Type
CSR Synopsis
Available IPD/Information URL
http://www.merck.com/clinical-trials/policies-perspectives.html
Learn more about this trial
Study to Test a Marketed Drug in the Treatment of Menstrual Migraine (0462-072)
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