Effect of Donepezil on the Reorganization of Cognitive Neural Network in Patients With Post-Stroke Cognitive Impairment

NCT ID: NCT00530478

Last Updated: 2007-09-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to demonstrate the efficacy and safety of donepezil on the recovery of cognitive function in patients with stroke and to delineate the neurophysiologic mechanisms of the therapeutic effect of donepezil on the recovery of cognitive network using functional neuroimaging technique.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Stroke

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Donepezil Stroke Cognitive function Cognitive neural network

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

NONE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Donepezil

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Ischemic stroke in the territory of right or left middle cerebral artery
* Post-onset duration of the recent-onset stroke is over 3 months
* Cognitive deficit ranged from 10 to 26 by minimal mental status examination (MMSE) score
* Disturbance in activities of daily living (ADL) ranged 0.5 \~ 2.0 by clinical dementia rating (CDR) scale

Exclusion Criteria

* Severe internal carotid artery stenosis on the lesion side
* Cardiac pacemaker or intracranial metal insertion
* Post-stroke seizure disorder or any evidence of epileptic spikes on electroencephalography (EEG)
Minimum Eligible Age

16 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Samsung Medical Center

OTHER

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Suk Hoon Ohn, MD, MS

Role: PRINCIPAL_INVESTIGATOR

Samsung Medical Center

Yun Hee Park, MD

Role: PRINCIPAL_INVESTIGATOR

Samsung Medical Center

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Samsung Medical Center

Seoul, Seoul, South Korea

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

South Korea

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Yun-Hee Kim, MD, PHD

Role: CONTACT

Phone: 82-2-3410-2818

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Yun-Hee Kim, MD, PHD

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2006-04-023

Identifier Type: -

Identifier Source: org_study_id