A Prospective, Multi-center, Single-arm Objective Performance Criteria Trial to Evaluate the Safety and Efficacy of Intracranial Thrombus Aspiration Catheter in Treatment of Acute Large-vessel Occlusive Stroke
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Aspiration
- Sponsor
- Sinomed Neurovita Technology Inc.
- Enrollment
- 26
- Locations
- 6
- Primary Endpoint
- Instant recanalization rate of target vessel after operation
- Status
- Terminated
- Last Updated
- 3 years ago
Overview
Brief Summary
A prospective, multicenter, single-arm objective performance criteria trial to investigate the safety and efficacy of SINOMED ADPAT for Recanalization Therapy in acute large-vessel occlusive stroke.
Detailed Description
This study plans to recruit 164 patients with acute intracranial large-vessel occlusion within 24 hours time window. The Primary endpoint is the instant recanalization rate of target vessel after operation. Secondary efficacy endpoints will include: 1) immediate recanalization rate of the first pass of aspiration; 2) the recanalization time of the target vessel blood flow; 3) the improvement of the postoperative NIHSS score; 4) the ratio of good neurological function (mRS 0-2 points) at 90 days; 5) the success rate of device; 6) the success rate of operation; 7) The proportion of rescue therapy. Safety endpoints will include: 1) the incidence of symptomatic intracranial hemorrhage within 24 hours after operation; 2) all-cause death and stroke-related mortality at 90 days; 3) stroke recurrence rate within 90 days after operation; 4) surgery-related complications; 5) adverse events; 6) serious adverse events; 7) Device defection rate
Investigators
Eligibility Criteria
Inclusion Criteria
- •Aged ≥ 18 years and ≤ 85 years;
- •Acute ischemic stroke, patients with anterior / posterior circulation vessel occlusion (intracranial segment of internal carotid artery or M1 or M2 segment of middle cerebral artery) confirmed by digital subtraction angiography (DSA);
- •Premorbid modified Rankin Scale(mRS)\<2 and Pre-operation NIHSS score ≥6;
- •The patients should receive endovascular treatment within 24 hours:
- •If the treatment could happen within 6 hours, the patient should have an CT or MR
- •If the treatment could happen 6-24 hours, the patient should have an CT or magnetic resonance (MR), have an ASPECTS ≥ 6 points. If immediate CT perfusion imaging or MR perfusion imaging is feasible, CT perfusion (CTP) or magnetic resonance perfusion (MRP) should be performed at the same time to assist in the evaluation of the infarct core.
- •Written informed consent obtained from patient or patient's legally authorized representative.
Exclusion Criteria
- •Large (more than one-third of the MCA) regions of clear hypodensity on the baseline neuroimaging or significant mass effect with midline shift;
- •Any type of intracranial hemorrhage or subarachnoid hemorrhage (only microbleeds are allowed, or judge from surgeon's clinical experience) by neuroimaging;
- •Proven Simultaneous acute occlusion of both carotid artery systems, and Proven tandem lesion of simultaneous occlusion of intracranial and extracranial vessels by neuroimaging;
- •Occlusion of the common carotid artery,and known or suspected chronic occlusion of target vessel;
- •Patients with consciousness disorder with posterior circulation vascular occlusion, NIHSS score is 3 points (1a=3);
- •Proven intracranial artery occlusion due to arterial dissection or arteritis by neuroimaging;
- •Arterial tortuosity and other problems that would prevent the device from reaching the target vessel;
- •Known to have one or more of the following allergies/resistances or contraindications: antiplatelet drugs/anticoagulant drugs/contrast agents and/or anesthetics;
- •Known allergies to medical devices and related products (allergy to materials such as nickel-titanium metal or its alloys);
- •Active bleeding or known bleeding tendency (such as: anticoagulant therapy or coagulation dysfunction before surgery, international normalized ratio (INR)\>3.0);
Outcomes
Primary Outcomes
Instant recanalization rate of target vessel after operation
Time Frame: Last aspiration
Instant recanalization rate (mTICI 2b-3) of target vessel after operation
Secondary Outcomes
- The recanalization time of the target vessel blood flow(Procedure time (femoral artery puncture to recanalization))
- Instant recanalization rate of target vessel after the first aspiration(First aspiration)
- The success rate of device(Intraoperative)
- The incidence of symptomatic intracranial hemorrhage(24(-6/+24) hours)
- The rate of Stroke recurrence(90 days)
- Procedure-related complications(Intraoperative)
- The improvement of the postoperative NIHSS score the improvement of the postoperative NIHSS score(Change in NIHSS score at preoperative、24(-6/+24) hours、7±2 days or discharge)
- Proportion of good neurological function (mRS 0-2)(90 days)
- The success rate of operation(End of Procedure)
- All-cause death and stroke-related mortality(90 days)
- Adverse events and serious adverse events(During the clinical trials)
- The rate of device defection(Intraoperative)