The Dutch Acute Stroke Trial: prediction of outcome with CT perfusion and CT angiography.
Completed
- Conditions
- stroke1000796310003216ischemic infarct
- Registration Number
- NL-OMON36955
- Lead Sponsor
- niversitair Medisch Centrum Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 1500
Inclusion Criteria
Acute neurological deficit caused by cerebral ischemia within 9 hours of onset.
No known contraindictations against intravenous contrast.
Informed consent.
Exclusion Criteria
Another diagnosis such as intracerebral hemorrhage, subarachnoid hemorrhage or tumor.
Known contrast allergy or renal failure.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>primary outcome measures will be 90 day outcome measured by modified Rankin<br /><br>Scale (mRS). </p><br>
- Secondary Outcome Measures
Name Time Method <p>Day 3 outcome (NIHSS and mRS) or earlier at discharge.<br /><br>Vessel recanalization on CTA.<br /><br>Final infarct size.<br /><br>Asymptomatic and symptomatic hemorrhage on CT. </p><br>