Randomized a Clinical Trial With Medical Device in Acute Ischemic Stroke

NCT07113184 · tracked via the Priya Life Science Spain tracker

Sponsor

Instituto de Investigación Marqués de Valdecilla

Phase

Not applicable

Started

2025-10-01

Last updated

2025-08-08

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

dual srsingle sr

dual sr: Dual Stentriever

single sr: Single Stentriever

Study summary

This study seeks to provide high-quality evidence on the potential benefits of the dual stentriever approach, potentially informing future clinical guidelines and improving outcomes in patients with anterior circulation large vessel occlusion strokes.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Age ≥ 18 * NIHSS ≥ 6 * mRS ≤ 1 * Proximal anterior circulation occlusion * ASPECTS \> 6 * Informed consent Exclusion Criteria: * Absence of occlusion * Posterior circulation stroke * Carotid dissection or tandem stenosis requiring treatment * Severe comorbidities or contraindications to imaging contrast

Primary outcome measure(s)

Time takes in achieving complete reperfusion after a single thrombectomy pass. — 24 hours or 48 hours after thrombectomy
To evaluate the superiority of the dual stentriever technique in achieving complete reperfusion after a single thrombectomy pass.

Trial sites (3)

Facility	City	Region
Hospital de Burgos	Burgos	Spain
Complejo Hospitalario de Salamanca	Salamanca	Spain
Hospital universitario marques de valdecilla	Santander	Spain

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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 NCT07113184 on ClinicalTrials.gov ↗ ← All trials in Spain