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临床试验/NCT05465122
NCT05465122进行中(未招募)不适用

Long-Term Observational Extension of Participants in the CREST-2 Randomized Clinical Trial

Mayo Clinic110 个研究点 分布在 2 个国家目标入组 2,480 人开始时间: 2022年7月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Mayo Clinic
入组人数
2,480
试验地点
110
主要终点
Stroke

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
35 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Currently active or graduated participants in the CREST-2 randomized trial
  • •Able to provide written informed consent by self
  • •Fluent in English or Spanish

排除标准

  • •Unable to provide written informed consent
  • •Inability to follow study procedures

研究组 & 干预措施

Intensive Medical Management Group - no CEA

Subjects assigned to the intensive medical management alone with no carotid endarterectomy (CEA) group in the CREST-2 study (NCT02089217)

干预措施: Intensive Medical Management (Other)

Carotid Stenting Group (CAS)

Subjects assigned to the intensive medical management with carotid stenting group in the CREST-2 study (NCT02089217)

干预措施: FDA-approved carotid stents (Procedure)

Carotid Stenting Group (CAS)

Subjects assigned to the intensive medical management with carotid stenting group in the CREST-2 study (NCT02089217)

干预措施: Intensive Medical Management (Other)

Carotid Endarterectomy Group (CEA)

Subjects assigned to the intensive medical management with carotid endarterectomy group in the CREST-2 study (NCT02089217)

干预措施: Carotid Endarterectomy (Procedure)

Carotid Endarterectomy Group (CEA)

Subjects assigned to the intensive medical management with carotid endarterectomy group in the CREST-2 study (NCT02089217)

干预措施: Intensive Medical Management (Other)

Intensive Medical Management Group - no CAS

Subjects assigned to the intensive medical management alone with no carotid stenting (CAS) group in the CREST-2 study (NCT02089217)

干预措施: Intensive Medical Management (Other)

结局指标

主要结局

Stroke

时间窗: 5 years

Number of participants to experience a stroke

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

James F. Meschia

Principal Investigator

Mayo Clinic

研究点 (110)

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