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Clinical Trials in Germany / NCT07357285
Recruiting Not applicable

Safety and Efficacy Evaluation of the iNstroke 4F Thromboaspiration Catheter in Patients With Acute Ischaemic Stroke Due to Primary Distal Medium Vessel Occlusions (DMVO)

NCT07357285 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2025-11-27
Last updated
2026-01-23

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

Thromboaspiration catheter

Thromboaspiration catheter: Patients to undergo thromboaspiration with iNstroke 4F

Study summary

Prospective, Single-arm, Multi-centre Study to Evaluate the Efficacy and Safety of the iNstroke 4F Thromboaspiration Catheter in Patients with Acute Ischaemic Stroke due to Primary Distal Medium Vessel Occlusions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Subjects aged ≥ 18 years. * Subjects with symptom onset up to 24 hours. * Isolated primary demonstrated occlusion in a distal medium vessel (Non-dominant or distal M2-MCA segment, M3 or M4 segments of MCA, A2-A3 segments of ACA, P1, P2 and P3 segments of PCA) identified by magnetic resonance angiography (MRA) or computed tomography angiography (CTA). * Baseline NIHSS score ≥5 assessed before the procedure. * Pre-stroke mRS score ≤ 2. * Subjects with an ASPECTS score ≥ 6. * Informed consent obtained in accordance with the applicable country-specific regulations and as approved by the Ethics Committee (EC). Exclusion Criteria: * Subjects aged \< 18. * Suspected secondary DMVO. Suspicion or evidence of primary LVO whether it has been treated or not with fibrinolytic therapy or mechanical thrombectomy that subsequently develops a DMVO. * Baseline NIHSS score \<5 assessed before the procedure. * Pre-stroke mRS score \>2. * Subjects with an ASPECTS score \<6. * Severe comorbidity and/or shortened life expectancy that will likely prevent improvement or follow up or that will render the procedure unlikely to benefit the patient. * Severe allergy to contrast media. * Subjects with intracranial atherosclerotic occlusive disease or extra- or intracranial dissection. * Medical history of thrombocytopenia (Platelets \<100,000). * Subjects with tandem occlusions (evidence of complete occlusion, high-grade stenosis or arterial dissection in the extracranial or petrous segment of the internal carotid artery). * Subjects with occlusions in multiple vessels (e.g., MCA-M3 and ACA-A2), whether or not they undergo mechanical thrombectomy. * Subjects with cancer (with or without metastases) who have a life expectancy of less than 6 months. * Subjects participating in a clinical trial at the moment of the inclusion. * Subjects with pre-existing neurological or psychiatric illness that could confound the neurological or functional assessments.

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
Universitätsklinikum Bonn Bonn Germany Not Yet Recruiting
Universitätsklinikum Schleswig-Holstein Kiel Germany Not Yet Recruiting
Klinikum Marburg Marburg Germany Not Yet Recruiting
Klinikum Nürnberg Nuremberg Germany Not Yet Recruiting
Knappschaftskrankenhaus Recklinghausen Recklinghausen Germany Recruiting
Semmelweis University Center Budapest Hungary Recruiting
Hospital Universitario Vall d'Hebron Barcelona Spain Recruiting
Hospital Universitario 12 de Octubre Madrid Spain Not Yet Recruiting
Hospital Universitario de Getafe Madrid Spain Not Yet Recruiting
Hospital Universitario La Paz Madrid Spain Not Yet Recruiting
Hospital Clínico Universitario Virgen de Arrixaca Murcia Spain Recruiting

More iVascular S.L.U. trials in Germany

Other trials for the same condition

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 NCT07357285 on ClinicalTrials.gov ↗ ← All trials in Germany