The Oslo Acute Reperfusion Stroke Study (OSCAR)
Recruiting
- Conditions
- Acute Ischemic Stroke
- Registration Number
- NCT06220981
- Lead Sponsor
- Oslo University Hospital
- Brief Summary
Prospective registry of clinical and radiological data in acute ischemic stroke patients after endovascular treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 1500
Inclusion Criteria
- Age 18 years or older
- Patients with ischemic stroke and cerebral arterial occlusion treated with endovascular revascularization.
- All stroke severities and vascular distributions are eligible.
- Informed written consent signed by the patient, verbal consent from the patient as witnessed by a non-participating health care person or consent by the signature of the patient's family must be provided before inclusion. Patients for whom no informed consent can be obtained will not be included in the study but will be treated according to standard guidelines.
Exclusion criteria:
• Patient not eligible for the study or not available for follow-up assessments (e.g. non- resident).
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Modified Rankin Scale Score 3 months Modified Rankin Scale Score (mRS), min 0, max 6
- Secondary Outcome Measures
Name Time Method Infarct volume 1 day Infarct volume (ml)
Incidence of symptomatic intracranial hemorrhage 1 day Incidence of symptomatic intracranial hemorrhage (SICH)
Volume of new areas of diffusion restriction 1 day Volume of new areas of diffusion restriction
National Institute of Health Stroke Scale Score discharge National Institute of Health Stroke Scale Score (NIHSS, min 0, max 42)
Death due to any cause 3 months Mortality
serious adverse events 3 months serious adverse events
Trial Locations
- Locations (1)
Oslo University Hospital
🇳🇴Oslo, Norway