Safety and Efficacy of Intracranial Thrombus Aspiration Catheter in the Treatment of Acute Large-vessel Occlusive Stroke

Sinomed Neurovita Technology

Status

Terminated

Conditions

Aspiration

Large-vessel Occlusion

Acute Ischemic Stroke

Treatments

Device: Intracranial Thrombosis Aspiration Catheter

Study type

Interventional

Funder types

Industry

Identifiers

NCT05101668

SINOMED ADPAT

Details and patient eligibility

About

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.

Full 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

Enrollment

26 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

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:
1. If the treatment could happen within 6 hours, the patient should have an CT or MR
2. 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);
Baseline platelet counts<40×10^9/L;
Severe heart, liver or kidney failure and other serious or terminal illness;
Accompanied by ST-segment elevation myocardial infarction or severe infection (endocarditis or sepsis);
Hypertension that cannot be controlled after treatment (Baseline blood pressure>185/110 mmHg);
Baseline blood glucose < 2.7 or > 22.2 mmol/L. after treatment;
Life expectancy less than 3 months;
Women who are pregnant or planning to pregnancy during half a year by taking medical history);
Dementia or psychiatric disease that would confound the neurological or functional evaluations;
Current participation in another drug or device research;
Other special situations which the researchers believe to be not suitable for enrollment.