Fluoxetine for Visual Recovery After Ischemic Stroke (NCT02737930) | Clinical Trial Compass
TerminatedPhase 2
Fluoxetine for Visual Recovery After Ischemic Stroke
Stopped: Slow recruitment and lack of funding to expand to other sites.
United States17 participantsStarted 2016-05
Plain-language summary
The purpose of this study is to determine whether fluoxetine, a selective serotonin reuptake inhibitor commonly used for depression, enhances visual recovery after an acute ischemic stroke.
Who can participate
Age range18 Years ā 85 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* MRI-confirmed acute ischemic stroke resulting in an isolated homonymous visual field loss.
Exclusion Criteria:
* Known hypersensitivity to fluoxetine or other selective serotonin reuptake inhibitors
* National Institutes of Health Stroke Scale score greater than 5
* Premorbid modified Rankin Scale score greater than 2
* Premorbid monocular or binocular visual field deficits
* Premorbid retinopathy or optic neuropathy
* Premorbid depression
* History of cognitive impairment, dementia, or neurodegenerative disorder
* History of seizure disorder
* History of mania or hypomania
* History of hyponatremia
* History of angle-closure glaucoma or elevated intraocular pressure
* Current alcohol abuse or impaired liver function
* Current use of an antidepressant medication
* Current use of a medication likely to have an adverse interaction with fluoxetine
* Current use of a medication likely to impair post-stroke recovery
* Contraindication to MRI
* Pregnancy or lactation
* Hemorrhagic transformation of the index stroke, resulting in mass effect
* Enrollment in another clinical trial at the time of the index stroke
What they're measuring
1
Percent Change in the Bionocularly Averaged Perimetric Mean Deviation