Ignite Creation Date:
2024-05-05 @ 5:09 PM
Last Modification Date:
2024-10-26 @ 9:28 AM
Study NCT ID:
NCT00393588
Status:
COMPLETED
Last Update Posted:
2017-07-02
First Post:
2006-10-27
Brief Title:
Magnetic Resonance Imaging to Detect Brain Damage in Patients With Multiple Sclerosis
Sponsor:
National Institute of Neurological Disorders and Stroke NINDS
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
The Use of Magnetic Resonance Imaging to Investigate Cortical Damage in Patients With Multiple Sclerosis and Correlation With Cognitive Dysfunction
Status:
COMPLETED
Status Verified Date:
2011-09-29
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will test the ability of magnetic resonance imaging MRI to detect damage in different parts of the brain in patients with multiple sclerosis and to see if cognitive problems in patients can be correlated with the presence of lesions or reduction in the size of certain part of the brain Healthy subjects will also be studied to compare findings in patients with those of normal volunteers
Healthy subjects and patients with multiple sclerosis who are between 18 and 60 years of age may be eligible for this study Patients must not have severe clinical disability and must have been receiving and responding to Interferon beta for at least 6 months prior to enrollment Candidates are screened with a medical history physical examination MRI and possibly evoked potential testing which measures the nervous system response to visual auditory and somatosensory stimulation
Participants have two MRI scans within 1 week inclusive of the one performed for screening MRI uses a magnetic field and radio waves to obtain images of body tissues and organs The scanner is a metal cylinder surrounded by a strong magnetic field During the MRI the subject lies on a table that can slide in and out of the cylinder Participants will be tested with magnet strengths of 15 and 3 Tesla the higher the Tesla the greater the ability to see brain changes Each scan may last up to 90 minutes In addition to the MRI scans participants undergo cognitive testing that measures memory and thought processes and complete forms that test and quantify fatigue level stress anxiety and depression
Healthy subjects and patients with multiple sclerosis who are between 18 and 60 years of age may be eligible for this study Patients must not have severe clinical disability and must have been receiving and responding to Interferon beta for at least 6 months prior to enrollment Candidates are screened with a medical history physical examination MRI and possibly evoked potential testing which measures the nervous system response to visual auditory and somatosensory stimulation
Participants have two MRI scans within 1 week inclusive of the one performed for screening MRI uses a magnetic field and radio waves to obtain images of body tissues and organs The scanner is a metal cylinder surrounded by a strong magnetic field During the MRI the subject lies on a table that can slide in and out of the cylinder Participants will be tested with magnet strengths of 15 and 3 Tesla the higher the Tesla the greater the ability to see brain changes Each scan may last up to 90 minutes In addition to the MRI scans participants undergo cognitive testing that measures memory and thought processes and complete forms that test and quantify fatigue level stress anxiety and depression
Detailed Description:
OBJECTIVE The study will evaluate cognitive impairment in patients with multiple sclerosis MS and correlate the degree of cognitive dysfunction as identified by scores obtained in multiple cognitive tests with measurements of cortical thickness cortical lesions and white matter disease on magnetic resonance imaging of brains of MS individuals
STUDY POPULATION Study population will consist of 49 patients with relapsing remitting or secondary progressive MS with superimposed relapses who have been treated with Interferon beta at fully tolerated dosages for at least six months and 49 healthy volunteers matched for gender age and educational level We expect to screen 65 individuals per arm in order to be able to enroll 49 individuals per arm thus meeting the requirements of the sample size calculations
DESIGN After screening clinical rating disability by the means of the Expanded Disability Status Scale EDSS score neurophysiological eg evoked potential tests and imaging examinations MS patients and healthy subjects will undergo a neuropsychological evaluation using the Minimal Assessment of Cognitive Function in Multiple Sclerosis MACFIMS and the Automated Neuropsychological Assessment Metrics ANAM and also a 3 Tesla magnetic resonance imaging MRI After 25 and after 50 of projected patients have been enrolled distribution in MACFIMS will be evaluated to ensure that a broad spectrum of cognitive ability is represented Cortical thickness cortical lesions and white matter damage metrics eg lesion load diffusion tensor and magnetization transfer MRI measures will be computed In order to exclude the hypothesis that the presence of fatigue anxiety and depression normally occurring in MS patients might interfere with their cognitive performance thus acting as confounding factors scales measuring fatigue and mental status will be administered in all subjects Scores obtained on these scales will be used as covariates in each of the statistical analyses performed in the present study to account for their possible effects
OUTCOME MEASURES The first outcome measure will be the MACFIMS and cortical thickness values Correlation between these two metrics will be initially performed Secondly cortical lesions as well as white matter lesions on T1 and T2 weighted images magnetization transfer ratios and diffusion tensor imaging metrics of lesional and normal appearing brain tissues will be computed and their impact in determining cognitive impairment will be determined Thirdly deep gray matter white matter and total brain volume measures will be computed and correlated with cognitive function measured by the MACFIMS Similarly correlations between clinical disability as measured by the EDSS score and cognitive impairment as well as between EDSS score and each of the RMI variables explored in the study will be performed Finally the level of correlation between MACFIMS and ANAM tests will be investigated
STUDY POPULATION Study population will consist of 49 patients with relapsing remitting or secondary progressive MS with superimposed relapses who have been treated with Interferon beta at fully tolerated dosages for at least six months and 49 healthy volunteers matched for gender age and educational level We expect to screen 65 individuals per arm in order to be able to enroll 49 individuals per arm thus meeting the requirements of the sample size calculations
DESIGN After screening clinical rating disability by the means of the Expanded Disability Status Scale EDSS score neurophysiological eg evoked potential tests and imaging examinations MS patients and healthy subjects will undergo a neuropsychological evaluation using the Minimal Assessment of Cognitive Function in Multiple Sclerosis MACFIMS and the Automated Neuropsychological Assessment Metrics ANAM and also a 3 Tesla magnetic resonance imaging MRI After 25 and after 50 of projected patients have been enrolled distribution in MACFIMS will be evaluated to ensure that a broad spectrum of cognitive ability is represented Cortical thickness cortical lesions and white matter damage metrics eg lesion load diffusion tensor and magnetization transfer MRI measures will be computed In order to exclude the hypothesis that the presence of fatigue anxiety and depression normally occurring in MS patients might interfere with their cognitive performance thus acting as confounding factors scales measuring fatigue and mental status will be administered in all subjects Scores obtained on these scales will be used as covariates in each of the statistical analyses performed in the present study to account for their possible effects
OUTCOME MEASURES The first outcome measure will be the MACFIMS and cortical thickness values Correlation between these two metrics will be initially performed Secondly cortical lesions as well as white matter lesions on T1 and T2 weighted images magnetization transfer ratios and diffusion tensor imaging metrics of lesional and normal appearing brain tissues will be computed and their impact in determining cognitive impairment will be determined Thirdly deep gray matter white matter and total brain volume measures will be computed and correlated with cognitive function measured by the MACFIMS Similarly correlations between clinical disability as measured by the EDSS score and cognitive impairment as well as between EDSS score and each of the RMI variables explored in the study will be performed Finally the level of correlation between MACFIMS and ANAM tests will be investigated
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 07-N-0014 | None | None | None |