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Randomized, double-blind, place-contrlled study of donepezil in post-stroke patients with chronic non-fluent aphasia

Randomized, double-blind, place-contrlled study of donepezil in post-stroke patients with chronic non-fluent aphasia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000942
Enrollment
Unknown
Registered
2010-06-29
Start date
2009-10-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-stroke patients with chronic non-fluent aphasia

Interventions

Group A:Oral administration of donepezil, the first month
Group B:Placebo 10mg / day.

Sponsors

Nanfang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 to 80 years; 2. The course of disease is more than three month; 3. Cortical-subcortical or subcortical lesions caused by infarction or hemorrhage; 4. The patients give the informed consent after detailed explanation of this study; 5. Vision and hearing capabilities that allowed compliance with testing procedures; 6. Medically stable condition.

Exclusion criteria

Exclusion criteria: 1. Dementia, psychiatric disorders and conscious disturbance; 2. Dysarthria; 3. Acute or serious pulmonary, gastrointestinal, renal, hepatic, endocrine, cardiovascular disease or cancer; 4. Epilepsy have not been controled; 5. Use of cholinesterase inhibitors and other N–methyl-D-aspartate antagonists within four weeks; 6. Pregnancy, lactation or intended pregnancy; 7. Have hydrochloride allergy history of donepezil.

Design outcomes

Primary

MeasureTime frame
Aphasia Quotien;

Countries

China

Contacts

Public ContactXiaojia Liu
xiaojialiu@126.com+86 13660007311

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026