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Effect of Fingolimod in acute ischemic stroke

Phase 2
Recruiting
Conditions
I63.00
Cerebral infarction due to thrombosis of unspecified precerebral artery
Acute Ischemic Stroke.
Registration Number
IRCT20220423054619N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Acute onset focal neurologic deficit
Age more then 18 years
referring to hospital in less than 4.5 hours

Exclusion Criteria

Age more than 80
History of moderate or severe cardiovascular condition
History of prior probable retinal problems
Active viral or bacterial infection
Suspicion of other neurologic conditions than CVA
No existing hyperdense lesion in entry CT scan consisting with hemorrhagic lesion

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ational Institutes of Health Stroke Scale. Timepoint: At entrance , first month and 6th month after intervention. Method of measurement: Neurologic examination of neurologist.;The Modified Rankin Scale (mRS) for neurologic disability. Timepoint: Neurologic examination of neurologist. Method of measurement: The Modified Rankin Scale (mRS) for neurologic disability.
Secondary Outcome Measures
NameTimeMethod
Hemorrhagic changes of stroke territory. Timepoint: 3th and 7th day after stroke. Method of measurement: CT scan by neurologist.
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