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RECRUITING
NCT06559475
NA

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

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

View on ClinicalTrials.gov

Summary

To Evaluate the Safety and Efficacy of the Super-Bore 8/7F Thrombosis Aspiration Catheter in the Treatment of Acute Intracranial Large Vessel Occlusion.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

360

Start Date

2024-12-16

Completion Date

2026-04-01

Last Updated

2024-12-18

Healthy Volunteers

No

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.

Locations (1)

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

Hefei, Anhui, China