Maxalt 10mg Plus Caffeine 75mg in the Acute Treatment of Migraine Headache
Primary Purpose
Migraine With Aura, Migraine Without Aura
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Maxalt 10mg MLT plus Caffeine 75mg
Maxalt 10mg MLT plus Placebo
Placebo + Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Migraine With Aura focused on measuring Migraine
Eligibility Criteria
Inclusion Criteria:
- Subject is 18-65 years of age
- Diagnosis of migraine with or without aura
- 1 year history of migraine with 1-6 migraine attacks per month in the the three months prior to screening
- Medication for migraine prevention with a stable dose for at least 1 month prior to screening
- Has successfully treated a migraine attack with a triptan medication
Exclusion Criteria:
- Confirmed or suspected ischemic heart disease
- History of congenital heart disease
- History of cerebrovascular disease, including stroke
- History of ischemic abdominal disease
- Uncontrolled hypertension
- History of epilepsy
- History of basilar or hemiplegic migraine
- Impaired hepatic or renal function
- Greater than 15 headache days per month
- Subjects on an MAOI
- Subjects taking and ergotamine, or ergot containing preventive medication
- Subject is pregnant, trying to become pregnant or breast feeing
- Evidence of alcohol or substance abuse in the last year
- History of caffeine withdrawal headache
- Consumes more than 275 mg of caffeine on daily basis from dietary and medication sources
- Taking propanolol
Sites / Locations
- Diamond Headache Clinic
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Placebo Comparator
Arm Label
1
2
3
Arm Description
Maxalt 10mg with Caffeine 75mg
Maxalt 10mg plus Placebo
Double placebo
Outcomes
Primary Outcome Measures
The comparative percentage of migraine attacks that produce pain free response at 2 hours in the Maxalt 10mg MLT plus caffeine 75mg arm versus the Maxalt 10mg MLT plus placebo caffeine versus double placebo.
Secondary Outcome Measures
The comparative percentage of attacks that produce pain relief at 2 hours.
The comparative percentage of attacks that produce a pain free response and do not require re-treatment during the subsequent 24 hours and are not associated with headache pain recurrence.
The comparative percentage of resolution of associated symptoms of migraine present at the time of treatment as well as achieving a pain free response within 2 hours with each of the treatments.
The comparative number of patients reporting adverse effects to study medication, the type of adverse events reported and the percentage of attacks that are associated with the adverse effect.
Patient global evaluation for each of the treatments
Full Information
NCT ID
NCT00471952
First Posted
May 8, 2007
Last Updated
April 24, 2012
Sponsor
Diamond Headache Clinic
Collaborators
Merck Sharp & Dohme LLC
1. Study Identification
Unique Protocol Identification Number
NCT00471952
Brief Title
Maxalt 10mg Plus Caffeine 75mg in the Acute Treatment of Migraine Headache
Official Title
Maxalt 10mg Plus Caffeine 75mg in the Acute Treatment of Migraine Headache
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
April 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Diamond Headache Clinic
Collaborators
Merck Sharp & Dohme LLC
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the effect of rizatriptan, alone or combined with caffeine for treating acute attacks of migraine.
Each subject will have 3 months to treat 3 acute migraine headache attacks. Each subject will be dispensed one box containing 3 packets of study medication labeled for Headache #1, Headache #2, or Headache #3. Each packet wil contain either Maxalt 10mg MLT or a Maxalt placebo (sugar pill), and a capsule containing either caffeine 75mg or a capsule containing placebo (sugar).
One headache will be treated with a combination of Maxalt 10mg MLT and caffeine.
Another headache will be treated with a combination of Maxalt 10mg MLT and a capsule containing placebo.
A third headache will be treated with just placebo.
Neither the subject, the study coordinator, or your study doctor will know in which order you will receive the three different treatments. This information is available in case of emergency.
Detailed Description
Oral Maxalt has an extensive record of providing relief of acute migraine headache with 2 hours in the vast majority of patients, especially when undertaken as an early intervention strategy. Caffeine has been demonstrated to have analgesic effects in patients treating tension type headache and is found as part of a combination including aspirin and acetaminophen as a treatment for acute migraine headache.
The mechanism by which Maxalt relieves migraine headache is believed to be through action on 5HT1B/1D receptors both on blood vessels as well as centrally. Caffeine may have effects on relief of migraine through modifying norepinephrine related mechanisms which have been suggested through clinical research. Patients commonly report that they may obtain partial or complete relief of their migraines by consuming the modest amounts of caffeine found in a cup of coffee. this is estimated to be approximately 100mg per cup. The analgesic effects of caffeine appear to be most significant in the first 3 hours after ingestion. Recent work suggests that intervention in migraine when the pain is still mild and has not persisted for a prolonged duration may increase the likelihood of complete migraine response. Therefore, the combination of the two agents with activity in migraine that work early in the migraine process, have good tolerability at the proposed doses and working via different mechanism may increase the likelihood of patients achieving better response with their migraine treatment than that which is currently available.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine With Aura, Migraine Without Aura
Keywords
Migraine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Maxalt 10mg with Caffeine 75mg
Arm Title
2
Arm Type
Active Comparator
Arm Description
Maxalt 10mg plus Placebo
Arm Title
3
Arm Type
Placebo Comparator
Arm Description
Double placebo
Intervention Type
Drug
Intervention Name(s)
Maxalt 10mg MLT plus Caffeine 75mg
Intervention Description
One migraine attack will be treated
Intervention Type
Drug
Intervention Name(s)
Maxalt 10mg MLT plus Placebo
Intervention Description
One migraine attack will be treated with Maxalt 10mg plus placebo
Intervention Type
Drug
Intervention Name(s)
Placebo + Placebo
Intervention Description
One migraine attack will be treated with double placebo
Primary Outcome Measure Information:
Title
The comparative percentage of migraine attacks that produce pain free response at 2 hours in the Maxalt 10mg MLT plus caffeine 75mg arm versus the Maxalt 10mg MLT plus placebo caffeine versus double placebo.
Time Frame
2 hours
Secondary Outcome Measure Information:
Title
The comparative percentage of attacks that produce pain relief at 2 hours.
Time Frame
2 hours
Title
The comparative percentage of attacks that produce a pain free response and do not require re-treatment during the subsequent 24 hours and are not associated with headache pain recurrence.
Time Frame
24 hours
Title
The comparative percentage of resolution of associated symptoms of migraine present at the time of treatment as well as achieving a pain free response within 2 hours with each of the treatments.
Time Frame
2 hours
Title
The comparative number of patients reporting adverse effects to study medication, the type of adverse events reported and the percentage of attacks that are associated with the adverse effect.
Time Frame
24 hours
Title
Patient global evaluation for each of the treatments
Time Frame
24 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Subject is 18-65 years of age
Diagnosis of migraine with or without aura
1 year history of migraine with 1-6 migraine attacks per month in the the three months prior to screening
Medication for migraine prevention with a stable dose for at least 1 month prior to screening
Has successfully treated a migraine attack with a triptan medication
Exclusion Criteria:
Confirmed or suspected ischemic heart disease
History of congenital heart disease
History of cerebrovascular disease, including stroke
History of ischemic abdominal disease
Uncontrolled hypertension
History of epilepsy
History of basilar or hemiplegic migraine
Impaired hepatic or renal function
Greater than 15 headache days per month
Subjects on an MAOI
Subjects taking and ergotamine, or ergot containing preventive medication
Subject is pregnant, trying to become pregnant or breast feeing
Evidence of alcohol or substance abuse in the last year
History of caffeine withdrawal headache
Consumes more than 275 mg of caffeine on daily basis from dietary and medication sources
Taking propanolol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederick G Freitag, DO
Organizational Affiliation
Diamond Headache Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Diamond Headache Clinic
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60614
Country
United States
12. IPD Sharing Statement
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Maxalt 10mg Plus Caffeine 75mg in the Acute Treatment of Migraine Headache
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