NCT06559475

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

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 360 (estimated)
• Sponsor: The First Affiliated Hospital of University of Science and Technology of China · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Acute Ischemic Stroke
• Endovascular Thrombectomy

Interventions

Type	Name	Description
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.

Timeline

• Start date: 2024-12-16
• Primary completion: 2025-12-01
• Completion: 2026-04-01
• First posted: 2024-08-19
• Last updated: 2024-12-18

Locations

1 site across 1 country: China