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A Survey for Assessment of Effectiveness of Fluoxetine on Motor Improvement in Ischemic Stroke Patients

A Survey for Assessment of Effectiveness of Fluoxetine on Motor Improvement in Ischemic Stroke Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201312088323N7
Enrollment
150
Registered
2014-01-09
Start date
2013-03-20
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

stroke. Middle cerebral artery syndrome

Interventions

Intervention 1: In case group we prescribed cap fluoxetin,20 mg, P.O. one time a day for 90 days. Intervention 2: In control group we prescribe a capsule with same size and color to fluoxetin ,(as pla
Treatment - Drugs
Placebo
In case group we prescribed cap fluoxetin,20 mg, P.O. one time a day for 90 days.
In control group we prescribe a capsule with same size and color to fluoxetin ,(as placebo) for 90 days.

Sponsors

Kermanshah University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: inclusion criteria: stroke in middle cerebral artery( documented with imaging) and the patient have a hemi or mono plegy or paresis?the patient was not comatose ? filling the agreemnet sheet with patient or a reliable attendant ? the patient is dischargable and not admitted in ICU ward exclusion criteria: death of patient with any cause in duration of study ? irregular use of drugs ? irregular return for reexaminations ? presence of seizure, severe diarrhea, vomiting, severe insomnia ? presence of metabolic disorder( hyperthyroidism, hepatic , renal, cardiac,...) ? past medical history of psychiatric disorder or severe depression before stroke ? presence of SAH, lobar ICH, brain tumor ? stroke in other vascular territories (MCA, ACA,...) ? simmultaneous use of MAO-i , Selegiline, Cyproheptadine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Motor deficit and psychiatric disorder. Timepoint: before study,day 45, day 90. Method of measurement: Hamilthon depression rating Scale(HDRS) for psychiatric disorders and Barthel Index( BI ) for motor assessment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Esmaeili M.D.

Kermanshah University of Medical Science

dr_omid_esmaeili@yahoo.com+98 83142763009

Outcome results

None listed

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