- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01471314
MRA/fMRI Study of Spontaneous Migraine
Functional MRI and MR Angiography Used in Spontaneous Migraine
The purpose of this study is to examine migraineurs during spontaneous migraine attacks without aura, using high resolution magnetic resonance imaging (MRI), to study following:
- Changes in resting state blood-oxygenation-level-dependent-signal (BOLD-signal) using functional MRI (fMRI).
- Changes in circumferences of intra- and extracranial arteries using MR-angiography (MRA).
- Changes in regional and global cerebral blood flow (CBF) using the arterial spin labeling (ASL) method.
Moreover to perform diffusion tensor imaging (DTI) scans during spontaneous migraine attacks.
The migraine specific drug sumatriptan will be given to relieve pain and the effect will be registered using MRA and fMRI if possible.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Contacts and Locations
Study Locations
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-
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Glostrup, Denmark, DK-2600
- Recruiting
- Glostrup Hospital, Faculty of Health Sciences, University of Copenhagen
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Contact:
- Faisal Amin, MD, PhD student
- Phone Number: +4538633066
- Email: famoam01@regionh.dk
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Migraine without aura according to IHS criteria.
Exclusion Criteria:
- Other primary headaches.
- Tension-type headache more than 5 days/month.
- Use of anti-pain medication before the scanning on the examination day.
- Pregnant or nursing women.
- Contraindication for MR scan.
- Anamnestic or clinical signs of cardiovascular or cerebrovascular disease, unregulated psychiatric disease or drug misuse.
- Other clinical conditions assessed by the examining doctor.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Spontaneous migraine
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Collaborators and Investigators
Collaborators
Publications and helpful links
Study record dates
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-C-2008-089
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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