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Clinical Trials/JPRN-UMIN000015272
JPRN-UMIN000015272
Completed
未知

Recovery by Endovascular Salvage for Cerebral Ultra-acute Embolism (RESCUE)-Japan Randomized Controlled Trial - RESCUE-Japan RCT

Department of Neurosurgery Hyogo College of Medicine0 sites200 target enrollmentOctober 1, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Acute ischemic stroke patients due to IC and M1 proximal occlusion who received intravenous rt-PA therapy within 4.5 hours after onset
Sponsor
Department of Neurosurgery Hyogo College of Medicine
Enrollment
200
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 1, 2014
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Department of Neurosurgery Hyogo College of Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\)Patients whose neurological symptoms improved and NIHSS is eight points or less after intravenous rt\-PA therapy. 2\)Patients whose mRS is 3 points or more before the onset. 3\)Patients with past history of lumbar puncture or arterial puncture that were difficult of hemostasis. 4\)Patients with intracranial tumor 5\)Patients with hypersensitivity to contrast agent. 6\)Patients with serious renal disease. 7\)Patients with malignant tumor. 8\)Patients with pregnancy or suspect of pregnancy, or during lactation. 9\)Patients with findings of acute myocardial infarction or pericarditis after myocardial infarction. 10\)Patients who cannot be followed for 3 months. 11\)Patients with past history of cerebral aneurysm, cerebral arteriovenous malformation, cerebral venous thrombosis, or moyamoya disease. 12\)Patients with other occlusions besides ICA or M1 proximal portion. 13\)Patients with arterial dissection complicating endovascular treatment. 14\)Patients with tortuous arteries that disturb navigation of the device to the target vessel. 15\)Patients considered inappropriate to participate in the study.

Outcomes

Primary Outcomes

Not specified

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