Study of Rizatriptan in the Treatment of Acute Attacks of Post-traumatic Headache in U.S. Military Troops (Maxalt)
Primary Purpose
Chronic Post-traumatic Headache
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Rizatriptan
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Post-traumatic Headache focused on measuring active duty, blast induced, headache
Eligibility Criteria
Inclusion Criteria:
- U.S. Army soldier with history of concussion while deployed to a combat zone. Concussion is defined as head trauma with all of the following:
- No loss of consciousness or loss of consciousness less than 30 minutes.
- Glasgow Coma Score 13-15 (if known)
- Symptoms or signs of concussion.
- Concussion was secondary to primary, secondary, or tertiary blast injury.
- Headaches started within 7 days of concussion.
- Headaches have occurred for more than 3 months but not more than 24 months since the precipitating concussion.
- Headaches occurred 3 to 14 days per month during each of the previous two months.
- Headaches are migraine type and possess three or more of the following migraine features:
- moderate or severe pain
- throbbing or pulsatile pain
- unilateral or asymmetric pain
- pain exacerbated by or interfering with routine physical activity
- nausea or vomiting
- photosensitivity and phonosensitivity
- Headaches last 4 or more hours without treatment.
- Males 18 to 49 years of age.
Migraine Disability Assessment Score (MIDAS) greater than 10 or Headache Impact Test-6 (HIT6) score greater than 60.
-
Exclusion Criteria:
- Patients with a history of migraine headaches prior to concussion will be excluded.
- Prior use of any triptan medication for headache.
- Use of non-opioid analgesic medications 15 or more days per month for the previous month.
- Use of opioid medications more than 10 days in the previous month.
- Alcohol consumption of more than two servings (a serving is 2 oz hard liquor, 5 oz wine, or 12 oz beer) per day or more than 3 servings at one time on a weekly basis.
- Taking two or more medications from the following medication classes: SSRI, SNRI, or TCA.
- Headache prophylactic medication is allowed but must remain unchanged during the study period.
- Patients with depression, defined as a PHQ-9 score greater than 15, will be excluded from study participation.
- PTSD is NOT an exclusion criterion. PTSD will be defined as a clinical diagnosis by a behavioral health provider or PTSD symptom checklist score of 50 or higher.
- Systolic BP > 140 or diastolic BP > 90 on repeated measurements.
- Active use of dihydroergotamine.
- Known coronary artery disease, prior myocardial infarction, history of stroke or TIA, or liver disease.
- Subjects who will not be available for study-related follow-up visits will be excluded.
- Patient has cognitive impairment defined as mini-mental status exam score less than 27.
- Patients undergoing a medical board for headache, sequelae of TBI, or psychiatric disorders will be excluded.
- Patients suspected of malingering, exaggerating symptoms, or non-compliance will be excluded from study participation.
- Patient has hemiplegic migraine or basilar migraine.
Sites / Locations
- Madigan Army Medical Center - Neurology Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
rizatriptan
Placebo
Arm Description
initial treatment with Maxalt-MLT 10 mg followed by treatment with placebo
Initial treatment with placebo followed by treatment with Maxalt-MLT 10 mg
Outcomes
Primary Outcome Measures
Headache Severity
proportion of subjects who obtain headache relief defined as no pain or mild pain two hours after dosing
Secondary Outcome Measures
24 hour Migraine Quality of Life score
proportions of subjects achieving complete headache relief at 2 hours, sustained headache relief at 24 hours, 24-hour Migraine Quality of Life score, disability 2 hours after dosing, occurrence of associated symptoms, and side effects.
Full Information
NCT ID
NCT01306266
First Posted
February 25, 2011
Last Updated
August 17, 2015
Sponsor
Henry M. Jackson Foundation for the Advancement of Military Medicine
Collaborators
Merck Sharp & Dohme LLC
1. Study Identification
Unique Protocol Identification Number
NCT01306266
Brief Title
Study of Rizatriptan in the Treatment of Acute Attacks of Post-traumatic Headache in U.S. Military Troops
Acronym
Maxalt
Official Title
A Randomized, Double-blind, Placebo-controlled, Crossover Trial of Rizatriptan 10 mg Oral Disintegrating Tablet for Treatment of Acute Attacks of Chronic, Blast-induced, Post-traumatic Headache in U.S. Military Troops
Study Type
Interventional
2. Study Status
Record Verification Date
August 2015
Overall Recruitment Status
Withdrawn
Study Start Date
February 2011 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
August 2011 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Henry M. Jackson Foundation for the Advancement of Military Medicine
Collaborators
Merck Sharp & Dohme LLC
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the study is to determine the effectiveness of rizatriptan for treating attacks of chronic post-traumatic headache.
Detailed Description
Chronic post-traumatic headaches develop in about one third of soliders who have had head trauma caused by a blast. A wide variety of pain medicines, including rizatriptan, are used to treat these headaches in clinical practice. However, the effectiveness has not been established by clinical research studies.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Post-traumatic Headache
Keywords
active duty, blast induced, headache
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
rizatriptan
Arm Type
Active Comparator
Arm Description
initial treatment with Maxalt-MLT 10 mg followed by treatment with placebo
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Initial treatment with placebo followed by treatment with Maxalt-MLT 10 mg
Intervention Type
Drug
Intervention Name(s)
Rizatriptan
Other Intervention Name(s)
Maxalt
Intervention Description
initial treatment with Maxalt-MLT 10 mg followed by treatment with placebo. Drug is to be taken at onset of a moderate or severe headache
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
sugar pill
Intervention Description
Initial treatment with placebo followed by treatment with Maxalt-MLT 10 mg at onset of a moderate or severe headache.
Primary Outcome Measure Information:
Title
Headache Severity
Description
proportion of subjects who obtain headache relief defined as no pain or mild pain two hours after dosing
Time Frame
2 hours
Secondary Outcome Measure Information:
Title
24 hour Migraine Quality of Life score
Description
proportions of subjects achieving complete headache relief at 2 hours, sustained headache relief at 24 hours, 24-hour Migraine Quality of Life score, disability 2 hours after dosing, occurrence of associated symptoms, and side effects.
Time Frame
24 hours
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
U.S. Army soldier with history of concussion while deployed to a combat zone. Concussion is defined as head trauma with all of the following:
No loss of consciousness or loss of consciousness less than 30 minutes.
Glasgow Coma Score 13-15 (if known)
Symptoms or signs of concussion.
Concussion was secondary to primary, secondary, or tertiary blast injury.
Headaches started within 7 days of concussion.
Headaches have occurred for more than 3 months but not more than 24 months since the precipitating concussion.
Headaches occurred 3 to 14 days per month during each of the previous two months.
Headaches are migraine type and possess three or more of the following migraine features:
moderate or severe pain
throbbing or pulsatile pain
unilateral or asymmetric pain
pain exacerbated by or interfering with routine physical activity
nausea or vomiting
photosensitivity and phonosensitivity
Headaches last 4 or more hours without treatment.
Males 18 to 49 years of age.
Migraine Disability Assessment Score (MIDAS) greater than 10 or Headache Impact Test-6 (HIT6) score greater than 60.
-
Exclusion Criteria:
Patients with a history of migraine headaches prior to concussion will be excluded.
Prior use of any triptan medication for headache.
Use of non-opioid analgesic medications 15 or more days per month for the previous month.
Use of opioid medications more than 10 days in the previous month.
Alcohol consumption of more than two servings (a serving is 2 oz hard liquor, 5 oz wine, or 12 oz beer) per day or more than 3 servings at one time on a weekly basis.
Taking two or more medications from the following medication classes: SSRI, SNRI, or TCA.
Headache prophylactic medication is allowed but must remain unchanged during the study period.
Patients with depression, defined as a PHQ-9 score greater than 15, will be excluded from study participation.
PTSD is NOT an exclusion criterion. PTSD will be defined as a clinical diagnosis by a behavioral health provider or PTSD symptom checklist score of 50 or higher.
Systolic BP > 140 or diastolic BP > 90 on repeated measurements.
Active use of dihydroergotamine.
Known coronary artery disease, prior myocardial infarction, history of stroke or TIA, or liver disease.
Subjects who will not be available for study-related follow-up visits will be excluded.
Patient has cognitive impairment defined as mini-mental status exam score less than 27.
Patients undergoing a medical board for headache, sequelae of TBI, or psychiatric disorders will be excluded.
Patients suspected of malingering, exaggerating symptoms, or non-compliance will be excluded from study participation.
Patient has hemiplegic migraine or basilar migraine.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay C Erickson, MD
Organizational Affiliation
U.S. Army Medical Corp. Madigan Army Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Madigan Army Medical Center - Neurology Clinic
City
Tacoma
State/Province
Washington
ZIP/Postal Code
98431
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Study of Rizatriptan in the Treatment of Acute Attacks of Post-traumatic Headache in U.S. Military Troops
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