Phase
Condition
Multiple Sclerosis
Scar Tissue
Memory Loss
Treatment
N/AClinical Study ID
Ages 18-55 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
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
Study Design
Study Description
Connect with a study center
The George Washignton University
Washington, District of Columbia 20037
United StatesSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.