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Starting soon Not applicable

Study Evaluating Toro 88 Super Bore Aspiration Catheter for Acute Ischemic Stroke

NCT07089355 · tracked via the Priya Life Science France tracker
Sponsor
Toro Neurovascular, Inc
Phase
Not applicable
Started
2025-07
Last updated
2025-07-28

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

Toro 88 Super Bore Aspiration Catheter

Toro 88 Super Bore Aspiration Catheter: The Toro 88 Super Bore Aspiration Catheter is a neurovascular device designed for clot aspiration during mechanical thrombectomy procedures.

Study summary

The goal of this pilot study is to evaluate the safety and efficacy of the Toro 88 Super Bore Aspiration Catheter in acute ischemic stroke patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged ≥ 18 and ≤ 90 years at the time of consent * Presenting with an acute ischaemic stroke for which symptoms (or last time seen as normal) are \< 24h * With occlusion of the ICA / the M1 segment of the MCA / a vertebral artery diameter ≥3.5mm / the basilar artery, defined by eTICI≤1 * Requiring endovascular treatment (mechanical thrombectomy) with or without intravenous thrombolysis * For whom the experimental device is the first-line treatment * Without pre-existing disability (mRS ≤3 and 6≤ NIHSS ≤30 before stroke) * Informed consent signed : * By the patient * Or consent by a family member/trusted support person if the patient's condition does not allow them to express their consent in writing (L1111-6) Exclusion Criteria: * Arterial dissection * Suspicion of vasculitis * Suspected intracranial stenosis near the occlusion site * Concomitant intracranial haemorrhage * Known coagulation disorder * Known coagulopathy * Known platelet count \<50,000/μL * Significant mass effect with midline shift * Suspicion or evidence of aortic dissection, septic embolus, or bacterial endocarditis * INR ≥ 3.0 * APTT ≥ 2 times normal * Systolic blood pressure \> 185 mmHg and/or diastolic blood pressure \< 110 mmHg * Blood glucose \< 50 mg/dL or \>400 mg/dL according to the last measurement taken before the procedure * Known allergy to contrast media * Occluded arteries in more than one large vascular territory (at least two of the left and right internal carotid arteries or the territory of a carotid artery and an artery of the vertebrobasilar system). * Pregnant or breast-feeding women (urine or serum pregnancy test negative at inclusion). * Adults under legal protection (L1121-8) * Persons deprived of their liberty by judicial or administrative decision, persons under psychiatric care under articles L3212-1 and L3123-1 and persons admitted to a health or social establishment for purposes other than research (L1121-6). * Participation in other interventional clinical research

Primary outcome measure(s)

  • Incidence of adverse events that may be associated with the use of the experimental device at 24-36h — From start of procedure to 24-36 hours post-procedure

Trial sites (1)

FacilityCityRegionStatus
Hôpital Fondation Adolphe de Rothschild Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07089355 on ClinicalTrials.gov ↗ ← All trials in France