About this trial
The purpose of this clinical trial is to evaluate the efficacy and safety of combined recanalization therapy in patients who cannot be recanalized by acute large vessel occlusive stroke. The main questions it aims to answer are:
1、Proportion of subjects with mRs score of 0-1 at 90 days after surgery
Participants will:
1、In acute large vessel occlusive stroke, if traditional means cannot be recanalized, combined recanalization surgery (including arteriotomy and thrombectomy, cerebrovascular bypass surgery) is performed.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age: 18-75.
According to the current guidelines, there is a MT indication.
Before stroke, mRS ≤2;
ASPECTS ≥6;
Disqualifiers
Comorbid hemorrhagic vascular disease such as intracranial aneurysm or vascular malformation or other planned cerebrovascular surgery that may alter cerebral hemodynamics or lead to stroke;
unstable angina or myocardial infarction, congestive heart failure within the previous 6 months;
Pregnancy or perinatal period;
Hematologic disorders resulting in coagulation disorders;
Trial design
Parallel
Treatments tested in this trial
Surgery
Procedure/SurgeryRecombined recanalization surgery
Treatment groups
Trial outcomes
Primary outcomes
Proportion of subjects with mRs score of 0-1 at 90 days after surgery
Secondary outcomes
Changes in NIHSS score at 24 hours after surgery, 7 days after surgery, 30 days after surgery and 90 days after surgery compared with baseline;
The mRs score changed from baseline at 90 days after surgery
Change from baseline in MOCA score at 90 days after surgery
Change from baseline in MMSE score at 90 days after surgery
Sponsors and contacts
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