Long-Term Observational Extension of Participants in the CREST-2 Randomized Clinical Trial
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
James F. Meschia
Principal Investigator
Mayo Clinic
