Last updated: November 11, 2021
Sponsor: Xuanwu Hospital, Beijing
Overall Status: Completed
Phase
3
Condition
Stroke
Carotid Artery Disease
Cerebral Ischemia
Treatment
N/AClinical Study ID
NCT01758614
XW125-S001
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age ranging between 18 and 65 years;
- Digital subtraction angiography imaging studies demonstrating occlusion of unilateralICA or MCA;
- Digital subtraction angiography imaging studies demonstrating less than 50% stenosisof any other vessels especially contralateral ICA and MCA;
- Modified Rankin Scales (mRS) 0-2;
- Qualifying TIA or ischemic stroke in the territory of the occluded ICA or MCA musthave occurred within the past 12 months;
- The most recent stoke attacked more than 3 weeks ago;
- The neurological deficit must be stable for more than 1 month;
- No massive cerebral infarction (>50% of the MCA territory) in CT or MRI study;
- CT Perfusion demonstrates "misery perfusion" ;
- Competent to give informed consent;
- Legally an adult;
- Geographically accessible and reliable for follow-up;
Exclusion
Exclusion Criteria:
- Other neurovascular disease (such as cerebral aneurysm or arteriovenous malformation)conditions likely to cause focal cerebral ischemia;
- Known unstable angina or myocardial infarction within recent 6 months;
- Pregnant or perinatal stage women;
- Blood coagulation dysfunction;
- Any diseases likely to death within 2 years;
- Past history of EC-IC bypass surgery;
- Any contraindications or allergy to aspirin or clopidogrel;
- Any heart disease likely to cause cerebral ischemia including prosthetic valves,infective endocarditis, atrial fibrillation, sick sinus syndrome, myxoma andcardiomyopathy with ejection fraction less than 25%;
- Allergy to iodine or radiographic contrast media;
- Serum creatinine > 3mg/dl;
- Uncontrolled diabetes mellitus (fasting blood glucose >16.7mmol/l);
- Uncontrolled hypertension (systolic BP >180 mmHg, diastolic BP>110 mmHg);
- Severe liver dysfunction [alanine transaminase (ALT) and/or aspartate aminotransferase (AST) > 3 times of normal level];
- Concurrent participation in any other experimental treatment trial;
- Any condition that in the surgeon's judgment suggests the patient an unsuitablesurgical candidate;
Study Design
Total Participants: 330
Study Start date:
June 06, 2013
Estimated Completion Date:
March 01, 2020
Study Description
Connect with a study center
Department of neurosurgery, Xuanwu hospital
Beijing, Beijing 100053
ChinaSite Not Available
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