Multiple Sclerosis Clinical Trial
Assessment of Deep Gray Matter Anatomic Changes in RRMS Patients Treated With Gilenya® With and Without Cognitive Impairment Over a 2 Year Period Using NeuroQuant, NeuroQuarc and ANAM
Summary
The purpose of the research study is to investigate whether the extent and severity of lesions in the brain as measured by special MRI techniques can distinguish between Multiple Sclerosis (MS) patients with or without memory impairment and also between MS patients and age matched healthy controls.
Full Description
Impairment in thinking or memory is frequently present in multiple sclerosis but there are difficulties finding changes on the Brain MRI that correlate with impairment in thinking and memory. This occurs because standard MRI is good for detecting some but not all abnormalities in the brain. Those lesions that we do see in the brain on standard MRI do not correlate with memory impairment or the source of disability in most RRMS patients. This occurs because RRMS symptoms mainly result from parts of the brain which have been hard to evaluate with MRI until now.
To gain more insight into the source of memory impairment, we plan to explore differences in brain volume that may be present in RRMS patients without thinking or memory problems compared with those who are impaired. A secondary objective will be to compare RRMS patients in general with healthy controls.
A new MRI technique called NeuroQuant which reliably defines the volume of those parts of the brain that are important for memory and thinking will be used. Neuropsychological testing will also be offered, at no cost, to those patients being treated with Gilenya® in order to help define the presence and extent of their memory impairment. Automated Neuropsychological Assessment Matrices (ANAM)looks at all functional brain systems and will be administered by a psychometrist over a period of 90 minutes.
Eligibility Criteria
Inclusion and Exclusion Criteria
RRMS Patients
Inclusion Criteria
Male and Female adult definite RRMS patients with or without cognitive complaint
Age range 18-55 years old
Patients treated with Gilenya® (fingolimod) and other immunomodulating MS therapies
Able to provide informed consent
Exclusion Criteria
Pregnant or breastfeeding women
Patients with an infectious disease
Patients with any other medical or neurological condition that could affect cognition
Inability to communicate in English
Patients with clinically or radiologically isolated syndrome (CIS, RIS)
Primary or Secondary Progressive forms of MS
Current or past medical, neurological or psychiatric disorders (other than MS)
Previous illicit substance dependence or substance abuse
Pulse or steroid therapy within 8 weeks or preceding evaluation
Current major depressive episode
Control Patients
Inclusion Criteria
Male and Female adult with normal brain MRI and Neurological Examination
Headaches or dizziness
Age range 18-55 years
Able to provide informed consent
Exclusion Criteria
Patients with an infectious disease
Patients with any other medical or neurological condition that could affect cognition
Inability to provide informed consent
Inability to communicate in English
Pregnant or breastfeeding woman
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There is 1 Location for this study
Washington District of Columbia, 20037, United States
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