RecruitingNot ApplicableNCT06559475

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

Enrollment

360 participants

Start Date

Dec 16, 2024

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Conventional thrombectomy device treatment group and a procedure called Super-Bore Thrombosis Aspiration Catheter treatment group for people with acute ischemic stroke and endovascular thrombectomy. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURESuper-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.

PROCEDUREConventional 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

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NCT06559475


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