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临床试验/NCT02304744
NCT02304744Unknown不适用

Utrecht Coronary Biobank (UCORBIO)

UMC Utrecht1 个研究点 分布在 1 个国家目标入组 3,000 人开始时间: 2011年10月最近更新:
适应症

试验速览

阶段
不适用
发起方
UMC Utrecht
入组人数
3,000
试验地点
1
主要终点
major adverse cardiovascular events [MACE] (Stroke, myocardial infarction, coronary revascularization, death)

研究概览

简要总结

UCORBIO enrolls patients who undergo coronary angiography (for any indication). The investigators draw blood at the moment of insertion of the procedural arterial catheter.

At the moment of inclusion indication, procedural details, risk factor status, medication use and quality of life (RAND-36 and EuroQoL) is assessed. Patients are then followed-up for the occurrence of major adverse cardiovascular events for 5 years. During the follow-up period patients receive a questionnaire every year to check for hospital admissions. The questionnaires at two and five years of follow-up are enriched with quality of life questionnaires (RAND-36 and EuroQoL).

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Coronary angiography

排除标准

  • Age < 18 years.

结局指标

主要结局

major adverse cardiovascular events [MACE] (Stroke, myocardial infarction, coronary revascularization, death)

时间窗: 5 years

Stroke, myocardial infarction, coronary revascularization, death.

次要结局

未报告次要终点

研究者

发起方
UMC Utrecht
申办方类型
Other
责任方
Principal Investigator
主要研究者

Crystel Gijsberts

MD

UMC Utrecht

研究点 (1)

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