Multiparametric MRI Study of Endogenous Analgesia and Prediction the Efficacy of Migraine Pharmacological Prevention
Primary Purpose
Migraine
Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Doluxetine
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Migraine focused on measuring migraine, pain, CPM, offset analgesia, fMRI
Eligibility Criteria
Inclusion Criteria:
- patients diagnosed with migraine based on the International Headache Society (IHS) criteria 1 that have >4 attacks/month, both with and without aura
Exclusion Criteria:
- patients receiving any migraine preventive treatment during last 3 months or prior treatment with amytriptiline
- other chronic pain conditions
- psychiatric, other neurological diseases, language barrier or cognitive dysfunction
Sites / Locations
- Rambam health care campus
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo
treatment
Arm Description
Duloxetine will be given in a daily dose of 30 mg for 5 weeks
Outcomes
Primary Outcome Measures
Therapeutic response to the analgesic drugs
The level of pain relief
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01470352
Brief Title
Multiparametric MRI Study of Endogenous Analgesia and Prediction the Efficacy of Migraine Pharmacological Prevention
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
November 16, 2011 (Actual)
Primary Completion Date
November 6, 2017 (Actual)
Study Completion Date
November 6, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
d_yarnitsky
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To delineate brain mechanisms that subserve EA in the healthy state and to identify alterations in mechanisms supporting EA in chronic pain and their therapeutic relevance. Individuals with migraine will be examined between episodes in order to assess basal alterations in the efficiency of spatial and temporal filtering of noxious information. This population provides the unique opportunity to examine such processes without confounds arising from ongoing pain.
Detailed Description
Pain is a uniquely individual experience that is powerfully shaped by the action of descending control mechanisms. These systems may play crucial roles in the moment-to-moment tuning of the sensitivity, spatial, and temporal response characteristics of nociceptive processing mechanisms during both acute and pathological pain states. However, these systems remain poorly understood in human subjects. The proposed research will use psychophysics and multiparametric MRI to (i) delineate the brain mechanisms that subserve and regulate endogenous analgesia (EA) in the healthy state and (ii) to identify alterations in mechanisms supporting EA in chronic pain and their therapeutic relevance. In both healthy subjects and chronic pain patients, EA will be probed using the DNIC (diffuse noxious inhibitory controls) and offset analgesia paradigms. Functional MRI will examine activation of brainstem mechanisms important in EA, while both functional and structural connectivity analyses will assess the regulation of these brainstem mechanisms by cerebral cortical regions involved in attention and affect. One pathological painful condition, migraine, will be examined since it allows changes in EA associated with chronic pain to be investigated between episodes of pain. Finally, EA and EA associated structural and functional parameters will be used to predict the efficacy of one compound, amitriptyline, to treat migraine in individual patients. Taken together, the proposed research will provide substantial insights into basic mechanisms supporting and regulating EA and can provide a foundation for mechanism-based individualized choice of therapy that may benefit all chronic pain patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine
Keywords
migraine, pain, CPM, offset analgesia, fMRI
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
179 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
treatment
Arm Type
Active Comparator
Arm Description
Duloxetine will be given in a daily dose of 30 mg for 5 weeks
Intervention Type
Drug
Intervention Name(s)
Doluxetine
Other Intervention Name(s)
duloxetine
Intervention Description
30 mg/d
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
sugar
Intervention Description
suger pill 30mg/d
Primary Outcome Measure Information:
Title
Therapeutic response to the analgesic drugs
Description
The level of pain relief
Time Frame
2 month
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
patients diagnosed with migraine based on the International Headache Society (IHS) criteria 1 that have >4 attacks/month, both with and without aura
Exclusion Criteria:
patients receiving any migraine preventive treatment during last 3 months or prior treatment with amytriptiline
other chronic pain conditions
psychiatric, other neurological diseases, language barrier or cognitive dysfunction
Facility Information:
Facility Name
Rambam health care campus
City
Haifa
Country
Israel
12. IPD Sharing Statement
Learn more about this trial
Multiparametric MRI Study of Endogenous Analgesia and Prediction the Efficacy of Migraine Pharmacological Prevention
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