跳至主要内容
临床试验/NCT04827316
NCT04827316招募中不适用

Clinical Utility and Outcome Prediction of Cardiovascular Computed Tomography (PREDICT-CT)

Insel Gruppe AG, University Hospital Bern1 个研究点 分布在 1 个国家目标入组 4,200 人开始时间: 2017年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
4,200
试验地点
1
主要终点
All-cause death.

研究概览

简要总结

In this study the investigators retrospectively and prospectively collect information from enrolled subjects undergoing CCTA and evaluate the association of cardiac and non-cardiac imaging with laboratory markers and clinical data including outcome.

详细描述

In this study the investigators retrospectively and prospectively collect information from enrolled subjects through a period of a total of 10 years to evaluate multidimensional associations between phenotypic manifestations of cardiovascular disease via CCTA and cardiac and non-cardiac imaging, serum biomarkers, demographic and clinical information, clinical presentation (cross-sectional), therapy changes (time-varying) and their ability to predict mortality and MACE (major adverse cardiac event ) (longitudinal) in patients clinically indicated for CCTA.

The aim is to establish a comprehensive cross-sectional, time-varying and longitudinal data collection for individuals undergoing clinically-indicated CCTA to date in order to apply novel multiparametric approaches to determine cardiovascular significance to clinically-important patient-centered events. For data collection this registry will follow a standard CRF (case report form) structure, so to enable the merging of this data-set with other international registries, which might contribute in overcoming some gaps of knowledge from previous CCTA studies.

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

  • Adult individual >18 years
  • Undergoing clinically indicated CCTA
  • Signed informed consent or waiver

排除标准

  • 未提供

结局指标

主要结局

All-cause death.

时间窗: 10 years

The primary endpoint is the time to first occurrence of death from all-causes.

次要结局

  • Other outcome(10 years)
  • Major adverse cardiovascular events (MACE)(10 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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