A Multicenter, Randomized Controlled Clinical Investigation to Evaluate the Safety and Effectiveness of the Super-Bore 8/7F Aspiration Catheters in the Treatment of Acute Intracranial Large Vessel Occlusion

NARecruitingINTERVENTIONAL
Enrollment

360

Participants

Timeline

Start Date

December 16, 2024

Primary Completion Date

December 1, 2025

Study Completion Date

April 1, 2026

Conditions
Acute Ischemic StrokeEndovascular Thrombectomy
Interventions
PROCEDURE

Super-Bore Thrombosis Aspiration Catheter treatment group

For the subjects randomized to the Super-Bore Thrombosis Aspiration Catheter treatment group, Mechanical thrombectomy will be performed using a Super-Bore 8/7F Thrombosis Aspiration Catheter.

PROCEDURE

Conventional thrombectomy device treatment group

For the subjects randomized to the conventional thrombectomy device treatment group, mechanical thrombectomy will be performed using a commonly used thrombectomy devices in clinic, except for Super-Bore 8/7F Thrombosis Aspiration Catheter.

Trial Locations (1)

Unknown

RECRUITING

The First Affiliated Hospital of University of Science and Technology of China, Hefei

All Listed Sponsors
lead

The First Affiliated Hospital of University of Science and Technology of China

OTHER