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Efficacy of Donepezil in treatment of acute ischemic stroke complications

Efficacy of Donepezil in treatment of acute ischemic stroke complications, a clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220430054710N1
Enrollment
50
Registered
2022-06-01
Start date
2022-07-23
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

cerebral ischemic stroke. Acute cerebrovascular insufficiency

Interventions

Intervention 1: Intervention group: During the first 24 hours after stroke, Donepezil tablets (Jalinous Company
Iran) will be administered orally at a dose of 5 mg and 10 mg per day. The drug will be administered daily, once a day for six months. The course of treatment will be as follows: during the first 4 we

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with acute ischemic stroke less than 24 hours after the onset of symptoms

Exclusion criteria

Exclusion criteria: More than 24 hours after the onset of symptoms before assigning patients to the control or treatment group transient ischemic attacks Parkinson disease restless legs syndrome heart failure syncope symptomatic bradycardia active asthma or obstructive pulmonary disease recent abdominal surgery recent gastrointestinal bleeding gastrointestinal ulcer renal failure current use of acetylcholinesterase inhibitors

Design outcomes

Primary

MeasureTime frame
Motor function following acute ischemic stroke. Timepoint: The first day of admission, three months and six months after the onset of stroke. Method of measurement: Functional Independence Measure and Wisconsin Gait scale.;Cognitive function following acute ischemic stroke. Timepoint: The first day of admission, three months and six months after the onset of stroke. Method of measurement: Mini–mental State Examination test and Alzheimer’s Disease Assessment Scale-Cognitive subscale.

Secondary

MeasureTime frame
Mortality. Timepoint: 6-month. Method of measurement: Patients' follow up after 6 months.;Donepezil related side effect. Timepoint: 1-month, 3-month and 6 month. Method of measurement: During one-month, three-month, and six-month follow-ups, patients will be evaluated for side effects of donepezil.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahmoud Yousefifard

Iran University of Medical Sciences

yousefifard20@gmail.com+98 21 8670 4771

Outcome results

None listed

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