Amitriptyline to Prevent Headache After Traumatic Brain Injury
|First Submitted Date ICMJE||May 10, 2013|
|First Posted Date ICMJE||May 17, 2013|
|Last Update Posted Date||October 12, 2017|
|Start Date ICMJE||April 2013|
|Primary Completion Date||February 2016 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
||Frequency and severity of headaches [ Time Frame: 90 days ]
Headache frequency and severity are the most frequently used measures of medication efficacy in headache research. We will measure the number of headaches per week and severity ratings (1-10)using headache diaries and report to research staff.
|Original Primary Outcome Measures ICMJE||Same as current|
|Change History||Complete list of historical versions of study NCT01856270 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE
|Original Secondary Outcome Measures ICMJE||Same as current|
|Current Other Outcome Measures ICMJE||Not Provided|
|Original Other Outcome Measures ICMJE||Not Provided|
|Brief Title ICMJE||Amitriptyline to Prevent Headache After Traumatic Brain Injury|
|Official Title ICMJE||Amitriptyline to Prevent Headache After Traumatic Brain Injury|
The investigators propose to conduct a 2-arm, open-label pilot study to determine if early treatment with amitriptyline will decrease the frequency and severity of headaches after mild traumatic brain injury (TBI). Amitriptyline is a tricyclic antidepressant that is commonly available and inexpensive. It is used as a first-line drug for primary headache prevention in a very low dose range of 10-50 mg.
The investigators hypothesize that early preventive treatment with amitriptyline will avert the development of chronic post-traumatic headache (PTH) as compared to rates of headache from a recent natural history study on PTH after mild TBI.
The investigators propose to enroll inpatient subjects from a Level I trauma center as well as from outpatient clinics and from the general community with a diagnosis of mild TBI. Subjects will be screened for current headache. After baseline assessment, 72 subjects with current headache will be randomized to one of 2 groups. Group 1 will immediately begin amitriptyline and or Group 2 will be followed and begin amitriptyline at Day 30. All subjects will be asked to complete a daily headache diary beginning on Day 1 of the study. A detailed medical history and headache survey will be completed. Subjects will have a scheduled stepped increase in the drug dosage every week for 3 weeks to the maximum study dosage of 50 mg. Weekly telephone calls will monitor for adverse events and compliance with the drug and headache diary. Clinic visits will occur at 30, 60 and 90 days. The 30 day clinic visit will include cognitive testing to assess for differences between groups and initiation of drug treatment for Group 2. Both 30 and 60 day visits will include review of headache diary, potential adverse effects, and pill counts. The 90 day visit will be for outcome assessment. In addition, the headache survey will be repeated by telephone at Day 180.
Research Hypothesis and Aims: The ultimate aim of this research is to determine whether early treatment using amitriptyline can prevent the development of chronic headache after TBI. This proposal is for preliminary work that will give some indication of the effect of amitriptyline and provide information needed to design a definitive study of the efficacy of amitriptyline for the prevention of chronic post-traumatic headache.
Specific Aim 1 is to conduct a two-arm open-label study to examine the effect of preventive treatment with amitriptyline on the frequency and severity of headache after mild TBI compared to that seen in our observational study on the natural history of headache after mild TBI.
Specific Aim 2 is to collect data needed for design of a Phase III study, including an estimate of effect size, the variability in the number of headache days in those with mild TBI, and determining a desirable initiation date for preventive treatment (e.g., week 1 or month 1 after injury).
Specific Aim 3 is to examine the feasibility of headache diary use in individuals with mild TBI.
Specific Aim 4 is to establish the safety and tolerability of amitriptyline for the prevention of headache after mild TBI.
Hypothesis: Preventive treatment of early headaches with amitriptyline after mild TBI results in decreased prevalence of recurrent headache (percent of participants having at least 1 headache/week) and severe headaches (percent of participants having headaches with an average pain of 5 or higher) at three months as compared to the frequency and severity of headache in those followed in the natural history study who received usual care.
Data Collection and Measures: Data collection will occur at enrollment, at each clinic visit, and at Day 180. An examiner blinded to group assignment will administer all measures at Clinic Visit 1 as cognition will be compared between groups at that time point; other assessment points will be unblinded.
Primary Outcome Measure: Frequency and severity of headaches at 90 days after study initiation.
Secondary Measures: Secondary measures are the Brief Pain Inventory, Analog Pain Scale, Pain Sites, Headache Impact Test-6 (HIT-6), Insomnia Severity Index (ISI), Patient Health Questionnaire-9 (PHQ-9), General Anxiety Disorder - 7 Item Scale (GAD-7), Alcohol Use Disorders Identification Test—Consumption (AUDIT-C), Rivermead Post-Concussion Symptom Questionnaire (RPQ), EuroQol, Health Survey Short Form-12® (SF-12), and Satisfaction with Life Scale. Caffeine use and drug use questions will be asked that will model the AUDIT questions. Additional measures will be obtained at baseline to characterize injury type and severity, medication use, and accompanying disorders.
Headache Diary: The subject will be asked to fill out a headache diary each day during the study to rate the frequency and severity of headache as well as some simple headache characterization.
Enrollment and Randomization: Informed consent will be obtained from the participant as approved by the Human Subjects Division of the University of Washington. Subjects will be randomized into one of two groups (Group 1: early start vs. Group 2: delayed start) using a computerized blocked randomization, stratified on headache severity (average severity of <4 vs. >5).
Medication administration and dosing adjustments: The study drug, amitriptyline, will be dispensed in medication containers clearly marked with the dosage and instructions to take at bedtime daily (separate containers for 10 mg, 25 mg, and 50 mg). Once randomized, Group 1 participants will be started on one 10 mg capsule each evening. The dosage will be adjusted upwards to 25 mg daily for Week 2 to a maximum of 50 mg daily by Week 3. Group 2 participants will be assessed on Clinic Visit 1 (Day 30) for current headache. If the participant has continued to have headaches (new or worse than pre-injury), he/she will have the same ramp-up schedule when the study drug is started at Day 30. Those in group 2 who do not have headaches at day 30 will be followed by phone and with headache diaries throughout the study including outcomes. If the perceived side effects of the study drug are intolerable at any time during the study, subjects will be asked to decrease the dosage to half a pill until a new prescription arrives. If side effects remain intolerable after 3 days on the lower dose, that subject will be discontinued from the study drug but followed in the study. Regardless of dose, the schedule for visits and testing will continue. Participants will be allowed to use rescue medications as needed for headache.
Compliance: Each dosage will be in a separate pill container and clearly marked. Compliance will be assessed during the weekly telephone follow-up calls and at the follow-up clinic visits. Pill counts will be performed at each visit. Adequate compliance will be considered 80% medication consumption.
Schedule of Visits: Baseline Hospital Visit. Measures administered will include an interim medical history form (diagnoses, current medications), headache survey, pain measures, HIT-6, PHQ-9, ISI, RPQ, and SF-12. After completion of baseline assessments, the research assistant will instruct the participant in the use of a daily headache diary. The research assistant will distribute the labeled study drug to each Group 1 participant and will instruct on use. Participants will be given a schedule for increasing the dose weekly. Subjects will be asked to keep their pill containers to turn in at the next clinic visit.
Telephone Follow-Up Calls 1-9 (between clinic visits). The research assistant will contact the participant weekly (Telephone Follow-Up Calls 1, 2, 3) after enrollment to check on completion of headache diary and to confirm frequency and severity of headaches during the preceding week, study drug use, and use of rescue medications. In the case of adverse effects which are bothersome to the patient (e.g., mild sedation, dry mouth, constipation), the dosage will be decreased by one dosage level or by ½ pill per day.
Clinic Visit 1 (Day 30). For all participants on this visit, vital signs will be obtained. Drug containers will be collected from Group 1 and headache diaries will be collected from all subjects. Measures administered on this visit will include an interim medical history form (new diagnoses, changes in medications), headache survey, pain measures, HIT-6, PHQ-9, ISI, RPQ,and SF-12. Neuropsychological tests will be given on this visit only. For Group 1, if the dosage was decreased secondary to minor adverse events in the interim, one of the study physicians will meet with the participant to decide whether to maintain a lower dose or have a second trial of returning to a higher dose of the study drug. The second month's supply of study drug will be dispensed at this visit. For Group 2 participants with headache, medications for the first month of treatment will be distributed along with a ramp-up schedule.
Clinic Visit 2 (Day 60). Vital signs will be obtained. Drug containers and headache diaries will be collected from all subjects. Measures administered on this visit will include an interim medical history form (new diagnoses, changes in medications), headache survey, pain measures, HIT-6, PHQ-9, ISI, RPQ, and SF-12. If the dosage was decreased secondary to minor adverse events in the interim, one of the study physicians will meet with the participant to decide whether to maintain a lower dose or have a second trial of returning to a higher dose of the study drug. The final month's supply of study drug will be dispensed at this visit.
Clinic Visit 3 (Day 90). This will be the final visit for the subjects. Vital signs will be obtained. Drug containers and headache diaries will be collected from all subjects. Measures administered on this visit will include an interim medical history form (new diagnoses, changes in medications), headache survey, pain measures, HIT-6, PHQ-9, ISI, RPQ,and SF-12.
Telephone Follow-Up Call 10. The research assistant will call the subject at Day 180 to administer the headache survey (which includes the HIT-6) and record current medications only.
Subject Withdrawal: Subjects may be discontinued from the study drug on their request or if the subject experiences an adverse effect sufficient to warrant withdrawal from the study drug, In the case of discontinuation, the reason for withdrawal will be recorded and the subject will be asked to continue to monitor their headaches with use of the headache diary.
Data Analysis Study Sample Size and Rationale: In a recent observational study, the investigators observed that of people with new or worse headaches at baseline assessment after mild TBI, 35% had 1 or more headaches per week at 3 months and a similar fraction had average headache pain severity of 6 or more on a 0 (no pain) to 10 (worst pain imaginable) scale. The study's two end points are: 1) reduction in the percent of people with baseline headaches that has one or more headaches per week at 3 months; and 2) the reduction in the percent of people with baseline headaches that experience headache severity of 6 or more on a scale from 0 to 10 at 3 months. It will be necessary for 65 cases to be followed to 3 months in order to have 80% power to reject the null hypothesis of a 35% headache rate if amitriptyline taken as a preventive yields 21% of subjects having 1 or more headaches per week (a 40% reduction in the percentage of people with frequent headaches at 3 months). Similar numbers are needed to confirm a like reduction in the percent of participants with severe headaches (average pain of 6 or greater). These are based on a 1-sided significance level of 0.05. Allowing for up to 10% attrition (7 subjects), the investigators will recruit and randomize 72 participants. Based on the previous natural history study, the investigators expect about 104 cases per year to have new or worse headaches at baseline assessment. The investigators expect 60% to meet the eligibility criteria and 60% of those to consent to participate, yielding 37 cases per year to randomize.
Aim 1. The primary intent-to-treat analysis will determine the proportion of participants with frequent (1 or more headaches per week) or severe (with average pain of 6 or higher) headaches combining both arms at 3 months. Each of these proportions will be compared to the rate of each recorded in our observational study using a normal approximation to the binomial (one-sided chi-squared test). In the previous observational study, the investigators observed 35% with at least 1 headache per week and 36% with headaches having average pain of at least 6 on a scale from 0 to 10. A one-sided significance level of 0.05 will be used. The investigators will also examine evidence for any differential benefit for amitriptyline started at baseline or 1 month to help decide which to use for the Phase III trial if this pilot suggests that is worthwhile.
Aim 2. Descriptive statistics will be used (means, standard deviations, proportions) to help in the planning of the Phase II trial.
Aim 3 (feasibility of use of a headache diary). This will be addressed by examining the number of participants who do not use their diary at all, have over 10% missing data, or who report different values on the phone calls than is shown in the diary. Different modes of completing the diary (paper, smart phone or web application) will be studied to see if any are more user friendly for this population.
Aim 4. Descriptive statistics will be used to summarize the occurrence of adverse events. The investigators will estimate the impact of amitriptyline on cognition by comparing the neuropsychological performance at 1 month of those started on the drug at baseline to those who start drug after the 1-month assessment. The mean difference on each test will be calculated with a 95% confidence interval.
|Study Type ICMJE||Interventional|
|Study Phase||Phase 2|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Intervention ICMJE||Drug: Amitriptyline
Participants with headache will be enrolled within the first 12 weeks after injury and will be randomly assigned to 2 groups (see Table 1 for summary of protocol). Group 1 will be assessed within 3 months of injury (baseline, Day 0) (when they will receive their initial ramp-up dosage containers; see Table 2 for dosing), Day 30 and Day 60 (to monitor compliance and distribute study drug), and for final outcome on Day 90. Group 2 will be assessed within 3 months of injury (baseline, Day 0) but will not receive medication until their Day 30 visit. Those in group 2 who report headache at Day 30 will receive their initial dosage container and will then be reassessed at Day 60 (to monitor compliance and distribute study drug) and Day 90 (final outcome).
Other Name: Elavil
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Completed|
|Completion Date||February 2016|
|Primary Completion Date||February 2016 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages||18 Years to 60 Years (Adult)|
|Accepts Healthy Volunteers||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||United States|
|Removed Location Countries|
|NCT Number ICMJE||NCT01856270|
|Other Study ID Numbers ICMJE||44274-B|
|Has Data Monitoring Committee||Yes|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement||
|Responsible Party||Jeanne Hoffman, University of Washington|
|Study Sponsor ICMJE||University of Washington|
|Collaborators ICMJE||Not Provided|
|PRS Account||University of Washington|
|Verification Date||May 2016|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP