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Clinical Trials/NL-OMON39683
NL-OMON39683
Recruiting
Phase 3

Multi Center Clinical trial of endovascular treatment of acute ischemic stroke in the Netherlands. - MR CLEA

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
brain infarct
Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Enrollment
500
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • \*A clinical diagnosis of acute stroke, with a deficit on the NIH stroke scale of more than 2 points.
  • CT or MRI scan ruling out intracranial hemorrhage.
  • Intracranial arterial occlusion of the distal intracranial carotid artery or middle (M1/M2\) or anterior (A1/A2\) cerebral artery, demonstrated with CTA, MRA or DSA.
  • The possibility to start treatment within 6 hours from onset.
  • Informed consent given.
  • Age 18 or over.

Exclusion Criteria

  • \- cerebral infarction in past 6 weeks
  • \-history in intracerebral bleeding
  • \-RR \> 185/110 unresponsive to antihypertensive agents
  • \-blood glucose of \< 2\.7 or \> 22\.2
  • \-Clinical signs of hemorrhagic diathesis or platelet count \<90 x 10\*9/L, APTT\>50 sec or INR \>1\.7
  • \- intravenous treatment with thrombolysis with a dose exceeding 0\.9mg/kg or 90 mg
  • \-patients who are treated with intravenous thrombolysis while having cantra\-indications for it.;Exclusion criteria for mechanical thrombectomy
  • \- carotid artery stenosis over 70% (NASCETT) which cannot be stented
  • \-RR \> 185/110
  • \-Blood glucose \< 2\.7 or \>22\.2

Outcomes

Primary Outcomes

Not specified

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