Diffusion Magnetic Resonance Imaging (dMRI) in the Early Evaluation of Brain White Matter Diseases
NCT ID: NCT07108712
Last Updated: 2025-08-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
150 participants
OBSERVATIONAL
2025-05-01
2025-12-01
Brief Summary
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Detailed Description
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Diffusion Magnetic Resonance Imaging (dMRI), has emerged as a powerful non-invasive imaging tool for evaluating microstructural changes in brain white matter. This protocol aims to investigate the role of dMRI in the early identification and characterization of brain white matter diseases, focusing on its potential for detecting abnormalities before the onset of overt clinical symptoms.
Diffusion-weighted imaging (DWI), one of the first advanced magnetic resonance imaging (MRI) techniques, has rapidly ascended on the basis of its applicability in strokes and some infectious diseases. Restricted diffusion is significant information in the context of vascular ischemia, helping to delimit the brain-damaged area
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Study group
Patients diagnosed with suspected early-stage white matter disease (e.g., multiple sclerosis, small vessel disease, Alzheimer's disease, frontotemporal dementia, leukoaraiosis) will be enrolled.
Magnetic Resonance Imaging (MRI)
Magnetic Resonance Imaging (MRI) Scanner: All imaging will be performed using a 1.5 tesla MRI scanner to ensure high resolution and signal-to-noise ratio.
Interventions
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Magnetic Resonance Imaging (MRI)
Magnetic Resonance Imaging (MRI) Scanner: All imaging will be performed using a 1.5 tesla MRI scanner to ensure high resolution and signal-to-noise ratio.
Eligibility Criteria
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Inclusion Criteria
* Clinical suspicion of early-stage white matter disease.
* No prior diagnosis of significant neurological disorders (e.g., stroke, brain tumors).
* Ability to provide informed consent.
Exclusion Criteria
* Contraindications for magnetic resonance imaging (MRI) (e.g., metal implants, pacemakers).
* Severe psychiatric or cognitive impairment that prevents participation.
* Control Group: Healthy individuals without any clinical history of neurological diseases, matched by age and sex to the patient cohort.
18 Years
80 Years
ALL
No
Sponsors
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The General Authority for Teaching Hospitals and Institutes
NETWORK
Responsible Party
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Hekmat Samir Baumey
Lecturer of Diagnostic Radiology, Damnhour National Medical Institute
Locations
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General Authority for Teaching Hospitals and Institutes
Cairo, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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HD000235
Identifier Type: -
Identifier Source: org_study_id
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