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Magnetic Resonance Imaging to Detect Brain Damage in Patients With Multiple Sclerosis

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by
National Institute of Neurological Disorders and Stroke (NINDS)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for Multiple Sclerosis focused on measuring White Matter, Grey Matter, Brain, Disability, Lesions, Multiple Sclerosis, MS, Healthy Volunteer, HV

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA - MULTIPLE SCLEROSIS PATIENTS: Diagnosis of clinically isolated syndrome or MS. Age between 18 and 55. EDSS between 0 and 6.5. EXCLUSION CRITERIA - MULTIPLE SCLEROSIS PATIENTS: Presence of clinical relapse at the time of the enrollment or within the previous 3 months. Concomitant systemic disorder or central nervous system diseases of any kind or other related risk factors. Previous history of alcohol and substances abuse. Medical contraindications for MRI. Psychological contraindications for MRI. Pregnancy. Unable to provide informed consent. INCLUSION CRITERIA - HEALTHY VOLUNTEERS: Age greater than 18 years. EXCLUSION CRITERIA - HEALTHY VOLUNTEERS: Systemic disorder or central nervous system diseases of any kind or other related risk factors. Previous history of alcohol and substances abuse. Medical contraindications for MRI. Psychological contraindications for MRI. Pregnancy. Unable to provide informed consent. INCLUSION CRITERIA - STROKE PATIENTS: Age greater than 18 years. Pure motor hemiparesis secondary to a first and single acute ischemic infarct localized in the white matter of the pyramidal tract (confirmation and location stroke by MRI). No other major diseases of the central nervous system or neurological signs. No other visible MRI lesions of the corticospinal tract on T2-weighted images (e.g., patients with white matter lesions on tracts not connected with the pyramidal tract and clinically silent will not be excluded). EXCLUSION CRITERIA - STROKE PATIENTS: Stroke onset less than 3 months prior to the study enrollment. Previous history of alcohol and substances abuse. Medical contraindications for MRI. Contraindications for MRI. Critical stenosis of either carotids or vertebrobasilar artery as demonstrated by a Transcranial Doppler. Pregnancy. Unable to provide informed consent.

Sites / Locations

  • National Institutes of Health Clinical Center, 9000 Rockville Pike

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
December 10, 2004
Last Updated
June 30, 2017
Sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
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1. Study Identification

Unique Protocol Identification Number
NCT00099307
Brief Title
Magnetic Resonance Imaging to Detect Brain Damage in Patients With Multiple Sclerosis
Official Title
An Exploratory Study on Detection of Cortical Damage in Patients With Multiple Sclerosis Using Magnetic Resonance Imaging
Study Type
Observational

2. Study Status

Record Verification Date
September 28, 2011
Overall Recruitment Status
Completed
Study Start Date
December 8, 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 28, 2011 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Neurological Disorders and Stroke (NINDS)

4. Oversight

5. Study Description

Brief Summary
This study will determine whether magnetic resonance imaging (MRI) can detect damage to certain parts of the brain and analyze the thickness of the brain's outer surface in patients with multiple sclerosis. MRI is a diagnostic test that uses a strong magnetic field and radio waves to obtain images of body organs and tissues. It can sometimes permit diagnosis even before symptoms develop. MS is a disease of white matter, the fatty covering around the nerves in the brain and spinal cord. The nerves themselves are called gray matter. Damage to white matter impairs nerve function, leading to a variety of symptoms, such as weakness, vision problems, difficulty walking, paralysis, and others. MRI can detect some changes in white matter, but changes that may also appear in gray matter may be more difficult to find. This study will use new MRI techniques to try to identify gray matter damage in patients with MS. Healthy volunteers and people with MS or clinically isolated syndrome (an early stage of MS in which the patient has had just one of the problems MS can cause) who are between 18 and 55 years of age may be eligible for this study. Candidates are screened with a medical history and neurological examination, and blood and urine tests. Within one month of the screening evaluation, participants undergo MRI scanning on a standard 1.5 Tesla machine to confirm their health status. (The power of the MRI scanner is measured in Tesla; the higher the Tesla, the better the visualization.) For this procedure, the subject lies on a table that moves into the scanner (a narrow cylinder with a magnetic field), and wears earplugs to muffle loud knocking and thumping sounds that occur during the scanning process. During the procedure, a contrast agent called Gadolinium is injected into the blood stream to brighten the images. The test lasts about 2 hours, during which time the subject must lie still for up to a few minutes at a time. Within a month after the first MRI, participants repeat the test for a second time. The procedure is identical to the first scan, except a 3.0 Tesla machine is used.
Detailed Description
OBJECTIVE: Detection of cortical lesions in patients with multiple sclerosis (MS) using magnetic resonance imaging (MRI) is challenging. Their identification might provide more insight in explaining the level of disability in patients with MS. Primary aim of the present study is identifying cortical lesions in patients with MS using MRI. As a secondary aim, correlation between cortical lesions presence and clinical disability score (i.e. Expanded Disability Status Score or EDSS scale) will be analyzed. Tertiary aims will be provided by the relationships between the presence of cortical lesions and reduction in cortical thickness and extent of remote white matter disease pathology. Additionally, the role of white matter lesions in causing remote pathology will be studied. To better characterize this damage, patients with previous stroke, presenting with a single lesion on the pyramidal tract will be enrolled and diffusion-derived indices of white matter remote tracts will be computed. STUDY POPULATION: Fifty patients with definite MS or with a single attack and an MRI suggestive of MS (i.e., clinically isolated syndrome) according to McDonald criteria, and 55 healthy volunteers will be enrolled. Fifteen patients with previous ischemic stroke and 15 age- and gender-matched healthy volunteers will also be enrolled. DESIGN: After a clinical evaluation and an MRI at 1.5 Tesla, each individual will be imaged once at 3.0 Tesla scan. Clinical MRI before and within 15 minutes after contrast injection will be obtained in each patient at both 1.5 and 3 Tesla scans. In addition, 3 spoiled gradient-echo sequence, diffusion tensor images and double inversion recovery sequences will be acquired on the 3 Tesla MRI. Some healthy volunteers (up to 15) and patients (up to 15) will be required to be imaged twice on the 3T magnet as to optimize the sequences of this study. Additionally, 20 patients in whom cortical lesions will be identified using the above-mentioned techniques and 20 healthy volunteers will undergo brain perfusion MRIs. This may represent the third 3T MRI for the former in some instances. OUTCOME MEASURES: In MS patients, the number of cortical lesions will be computed. The EDSS score will serve for investigating the relationship between cortical lesions and clinical disability. Effect of cortical or white matter lesions in causing remote degeneration will be studied using diffusion tensor and magnetization transfer imaging in patients with both stroke and MS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
White Matter, Grey Matter, Brain, Disability, Lesions, Multiple Sclerosis, MS, Healthy Volunteer, HV

7. Study Design

Enrollment
94 (Actual)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA - MULTIPLE SCLEROSIS PATIENTS: Diagnosis of clinically isolated syndrome or MS. Age between 18 and 55. EDSS between 0 and 6.5. EXCLUSION CRITERIA - MULTIPLE SCLEROSIS PATIENTS: Presence of clinical relapse at the time of the enrollment or within the previous 3 months. Concomitant systemic disorder or central nervous system diseases of any kind or other related risk factors. Previous history of alcohol and substances abuse. Medical contraindications for MRI. Psychological contraindications for MRI. Pregnancy. Unable to provide informed consent. INCLUSION CRITERIA - HEALTHY VOLUNTEERS: Age greater than 18 years. EXCLUSION CRITERIA - HEALTHY VOLUNTEERS: Systemic disorder or central nervous system diseases of any kind or other related risk factors. Previous history of alcohol and substances abuse. Medical contraindications for MRI. Psychological contraindications for MRI. Pregnancy. Unable to provide informed consent. INCLUSION CRITERIA - STROKE PATIENTS: Age greater than 18 years. Pure motor hemiparesis secondary to a first and single acute ischemic infarct localized in the white matter of the pyramidal tract (confirmation and location stroke by MRI). No other major diseases of the central nervous system or neurological signs. No other visible MRI lesions of the corticospinal tract on T2-weighted images (e.g., patients with white matter lesions on tracts not connected with the pyramidal tract and clinically silent will not be excluded). EXCLUSION CRITERIA - STROKE PATIENTS: Stroke onset less than 3 months prior to the study enrollment. Previous history of alcohol and substances abuse. Medical contraindications for MRI. Contraindications for MRI. Critical stenosis of either carotids or vertebrobasilar artery as demonstrated by a Transcranial Doppler. Pregnancy. Unable to provide informed consent.
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11936491
Citation
McFarland HF. The emerging role of MRI in multiple sclerosis and the new diagnostic criteria. Mult Scler. 2002 Feb;8(1):71-2. doi: 10.1177/135245850200800114. No abstract available.
Results Reference
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PubMed Identifier
11359721
Citation
Li DK, Zhao G, Paty DW. T2 hyperintensities: findings and significance. Neuroimaging Clin N Am. 2000 Nov;10(4):717-38 ,ix.
Results Reference
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PubMed Identifier
1859184
Citation
Harris JO, Frank JA, Patronas N, McFarlin DE, McFarland HF. Serial gadolinium-enhanced magnetic resonance imaging scans in patients with early, relapsing-remitting multiple sclerosis: implications for clinical trials and natural history. Ann Neurol. 1991 May;29(5):548-55. doi: 10.1002/ana.410290515.
Results Reference
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Magnetic Resonance Imaging to Detect Brain Damage in Patients With Multiple Sclerosis

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