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CEST-PROTECT: Proximal Flow Control With a Balloon Guide Catheter Plus Distal Embolic Protection: a Randomised, Open-label Trial Evaluating Cerebral Protection Techniques

Study acronym: CEST-PROTECT
StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Study First Submitted
Xuanwu Hospital, Beijing
204 trials monitored
See 3 trials at risk
Stroke
3,531 trials monitored
See 153 trials at risk
This randomized controlled trial aims to evaluate whether a proximal-distal dual cerebral protection strategy can reduce the occurrence of new cerebral ischemic lesions compared with a single cerebral protection strategy in patients undergoing carotid artery stenting. Eligible participants will be randomly assigned to receive either dual cerebral protection using proximal flow control combined with a distal embolic protection device or conventional single cerebral protection. Brain magnetic resonance imaging will be performed after the procedure to assess new ischemic lesions. The study will also evaluate peri-procedural neurological events and other safety and efficacy outcomes.
Trial Details
NCT Number NCT07841132
Lead Sponsor Xuanwu Hospital, Beijing
Collaborators: Union hospital of Fujian Medical University, Fujian Zhangzhou hospital, People's Hospital of Gaomi City, The First Affiliated Hospital of Haerbin Medical University, Henan Provincial People's Hospital, Heze Municipal Hospital, Jiangsu Provincial People's Hospital, Linyi People's Hospital, The First People's Hospital of Mianyang, Nanyang Central Hospital, Shandong Provincial Hospital, Shanxi Cardiovascular Hospital, Jinan Hospital, Xuanwu Hospital, Capital Medical University, Tianjin Huanhu Hospital, Chinese Academy of Medical Sciences, Fuwai Hospital, Xinqiao Hospital, Baoji third people's hospital, Liaocheng People's Hospital, Liaocheng Brains Hospital / Liaocheng People's Hospital
Conditions
(from sponsor)		 Carotid Artery Stenosis (Symptomatic and Asymptomatic)
Related terms Carotid Stenosis, Stroke
Enrollment 500 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov