Endovascular Revascularization for Chronic Carotid Artery Occlusion Trial

NARecruitingINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

May 17, 2017

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Carotid Occlusion
Interventions
DEVICE

Endovascular revascularization

All interventions will be performed via 8F femoral sheath. Target common carotid artery will be engaged with 8F JR 4 guiding catheter. Intra-luminal wiring using coronary guidewires and microcatheters or alternative subintimal tracking with antegrade re-entry technique. Wiring would be abandoned after 30 minutes of futile effort, consumption of more than 300 ml of contrast, or when the wire tip is confirmed to be extravascular. Once wire enters distal true lumen, the microcatheter was exchanged to a 1.5 mm diameter coronary balloon for pre-dilatation. Distal embolic protection device would be deployed if an adequate landing zone can be identified. Properly sized balloon expandable stents and self-expanding stents were then deployed to scaffold the occlusion. Balloon post-dilatation may be done if stent expansion was inadequate.

Trial Locations (1)

10002

RECRUITING

National Taiwan University Hospital, Taipei

All Listed Sponsors
lead

National Taiwan University Hospital

OTHER