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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00315367
Other study ID # MSA1-904
Secondary ID
Status Completed
Phase Phase 4
First received April 14, 2006
Last updated October 15, 2007
Start date September 2004
Est. completion date October 2007

Study information

Verified date October 2007
Source Neurognostics
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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.


Description:

Donepezil HCI (Aricept®) is an FDA-approved drug now used to enhance memory in patients with Alzheimer's disease. The aim of this project is to examine the effects of Donepezil HCI (Aricept®) on memory induced brain activation patterns in the context of a double-blind, crossover trial of patients with multiple sclerosis (MS). We will perform task activation experiments involving two cognitive domains. The proposed work on MS patients should yield new information regarding functional anatomic relationships during cognitive activity, and how these relationships change as a function of drug treatment.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Donepezil HCI (drug)


Locations

Country Name City State
United States Medical College of Wisconsin Milwaukee Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
Neurognostics

Country where clinical trial is conducted

United States, 

References & Publications (1)

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

Outcome

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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