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Long-Term Observational Extension of Participants in the CREST-2 Randomized Clinical Trial
The purpose of this Long-Term Observational Extension of Participants in the CREST-2 Randomized Clinical Trial (C2LOE - ClinicalTrials.gov Identifier: NCT02089217) study is to study is to assess post-procedural efficacy of carotid endarterectomy and carotid stenting.
Atherosclerotic plaque in the carotid arteries is responsible for 10 to 15% of all ischemic strokes. The ongoing NINDS-funded CREST-2 multicenter randomized clinical trial is testing whether in the short term (up to 4 years after study entry) procedural revascularization improves stroke prevention above and beyond what can be achieved with intensive medical management of vascular risk factors, especially hypertension and hyperlipidemia. Our proposal is for an observational extension of the CREST-2 clinical trial to test whether revascularization improves stroke prevention in the clinically relevant long term (up to 8 to 10 years). The current application proposes to use a site-less, centralized telephone approach to extend the follow-up of CREST-2 trial participants for assessing the primary study outcome (stroke) for up to 10 years. The average follow-up will increase from between 2-3 years (clinic-based randomized trial) to 7-8 years (observational extension). Each patient will be contacted by telephone at 6-month intervals, and queried regarding all hospitalizations since the last contact. Suspected stroke events will be adjudicated by an expert clinical events committee based on medical record review.
Age
35 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Alabama at Birmingham
Birmingham, Alabama, United States
Mayo Clinic Pheonix
Phoenix, Arizona, United States
Banner University Medical Center
Tucson, Arizona, United States
Central Arkansas VA
Little Rock, Arkansas, United States
Mission Cardiovascular Research Institute
Fremont, California, United States
Kaiser Permanente Los Angeles
Los Angeles, California, United States
USC/Keck Medical Center
Los Angeles, California, United States
University of California Los Angeles
Los Angeles, California, United States
Kaiser Permanente Divsion of Research
San Francisco, California, United States
Kaiser Permanente San Francisco
San Francisco, California, United States
Start Date
July 5, 2022
Primary Completion Date
February 28, 2026
Completion Date
February 28, 2026
Last Updated
September 5, 2025
2,480
ESTIMATED participants
Carotid Endarterectomy
PROCEDURE
FDA-approved carotid stents
PROCEDURE
Intensive Medical Management
OTHER
Lead Sponsor
Mayo Clinic
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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