Relapsing-Remitting Multiple Sclerosis Clinical Trial
Official title:
A Double-Blind, Crossover Trial of Aricept® in Memory-Impaired Patients With Multiple Sclerosis: A Phase IV Demonstration of Functional MRI (fMRI) as a Surrogate Marker of Brain Activity Associated With Improvement in Memory Function
Verified date | October 2007 |
Source | Neurognostics |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
The purpose of this study is to determine if medication designed to improve memory will help patients with Multiple Sclerosis (MS) who are experiencing memory problems using fMRI to track brain activity.
Status | Completed |
Enrollment | 26 |
Est. completion date | October 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Between 18 and 65 years of age and experiencing some forgetfulness - Diagnosed with MS, currently taking Rebif® and experiencing mild memory problems - Participants will have stable medication dosages 1 month prior to testing - With no past or present neurological disorders (e.g. head trauma, seizures, encephalitis, stroke) except MS - With no known medical illnesses (e.g. diabetes, uncontrolled hypertension, arthritis) - With no psychiatric illness - With no current substance abuse - Females should not be pregnant or nursing - With no metallic devices in the body or claustrophobia Exclusion Criteria: - Previous history of CNS disturbance other than MS - Severe motor or visual impairment that might interfere with the cognitive activation tasks - Prescribed psychoactive medications - Memory deficits caused by other significant neurological disease or psychiatric disorder - Active malignancy within one year of study participation - Known human immunodeficiency virus (HIV) - Current diagnosis of unstable glaucoma; history of myocardial infarction - Symptomatic Coronary Artery Disease within the last 12 months or evidence of ongoing ischemia or uncontrolled atrial or ventricular arrhythmias as shown by ECG; poorly controlled or labile hypertension - History of epilepsy or other seizure disorder within the past 12 months - Allergy or hypersensitivity to amphetamines or other sympathomimetic amines |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Medical College of Wisconsin | Milwaukee | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Neurognostics |
United States,
Krupp LB, Christodoulou C, Melville P, Scherl WF, MacAllister WS, Elkins LE. Donepezil improved memory in multiple sclerosis in a randomized clinical trial. Neurology. 2004 Nov 9;63(9):1579-85. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anatomic relationships during cognitive activity, and how these relationships change as a function of drug | |||
Secondary | fMRI as a surrogate marker for drug efficacy |
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