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NOT YET RECRUITING
NCT06614972

Balloon-expandable DES for ICAS Registry Study (BDES-ICAS Registry)

Sponsor: RenJi Hospital

View on ClinicalTrials.gov

Summary

To study the clinical outcomes after implantation of balloon-expandable drug-eluting stents in patients with symptomatic intracranial atherosclerotic stenosis in prevention of composite event of any stroke and death within 30 days and ischemic stroke in the territories of the responsible artery from 31 days to 1-year.

Official title: Clinical Outcome of Balloon-Expandable Drug-Eluting Stenting For Patients With Intracranial Atherosclerotic Stenosis: a Prospective, Multicenter, Real-World Registry Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

520

Start Date

2024-09-30

Completion Date

2030-09-30

Last Updated

2024-09-26

Healthy Volunteers

No

Interventions

DEVICE

Balloon-expandable drug-eluting stent

Balloon-expandable drug-eluting stent (BDES) is the device comprises of a balloon expandable sirolimus eluting stent and a delivery catheter that features a rapid exchange catheter design with a semi-compliant balloon located at its distal end.