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Comparison of the effects of Citalopram Versus Fluoxetine on motor function after stroke.

Comparison of the effects of Citalopram Versus Fluoxetine on motor recovery after stroke: A double-blind placebo-controlled randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141116019971N3
Enrollment
90
Registered
2017-12-03
Start date
2015-01-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Cerebral infarction. Sequelae of cerebral infarction

Interventions

Intervention 1: Group A: participants were received capsules containing 20 mg of Fluxetine orally, daily for 90 days, as well as physiotherapy sessions 1 hour per day, 5 days per week, for 12 weeks. I
Treatment - Drugs
Group A: participants were received capsules containing 20 mg of Fluxetine orally, daily for 90 days, as well as physiotherapy sessions 1 hour per day, 5 days per week, for 12 weeks.
Group B: participants were received capsules containing 20 mg of Citaloprem orally, daily for 90 days, as well as physiotherapy sessions 1 hour per day, 5 days per week, for 12 weeks.
Control group: participants were received capsules containing microcrystalline cellulose, orally, daily for 90 days, as well as physiotherapy sessions 1 hour per day, 5 days per week, for 12 weeks.

Sponsors

Vice chancellor for research, Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Over 18 years of age Suffering from hemiparesis or hemiplegia as a result of a first-time acute (in the past 24 hours) ischemic stroke An initial Fugl-Meyer Motor Scale score of under 55

Exclusion criteria

Exclusion criteria: A National Institutes of Health Stroke Scale score of less than five Prior disabilities including aphasia, cognitive disorders and motor disorders due to stroke or any other neurodegenerative disease Pregnancy or breastfeeding Currently taking antidepressants Contraindications of therapy, including renal insufficiency (glomerular filtration rate <30 ml/min), abnormal liver function tests, hyponatremia and a long QT interval on an electrocardiogram and Any significant adverse effects (agitation, hypertension or other signs of serotonin syndrome) after initiation of treatment

Design outcomes

Primary

MeasureTime frame
Motor function. Timepoint: At recruitment and after 90 days. Method of measurement: Fugl-Meyer Motor Scale score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan Karimialavijeh

Tehran University of Medical Sciences

drkarimi86@gmail.com+98 21 84901

Outcome results

None listed

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