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临床试验/NCT00932958
NCT00932958已完成不适用

Physicians International CCTA Utilization Registry

MDDX LLC1 个研究点 分布在 1 个国家目标入组 6,000 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
MDDX LLC
入组人数
6,000
试验地点
1
主要终点
CCTA utilization parameters and clinical findings

研究概览

简要总结

This protocol describes an observational study whose goal is to collect de-identified Coronary CT Angiography (CCTA) acquisition factors and interpretations (findings) from several hundred U.S. and international imaging facilities. The study uses an electronic data capture tool to collect de-identified CCTA utilization parameters and clinical findings in order to create a multi-center registry. This registry will be used for scientific analysis and publication of pertinent medical trends such as CT utilization, radiation dose, and common cardiovascular findings. The registry will be used to determine areas of interest for future randomized controlled trials.

All data will be collected with patient identifiers removed and in complete accordance with HIPAA regulations. All data will be analyzed in aggregate, thus further minimizing the risk of patient confidentiality violations.

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 participants who are able and willing to consent for themselves
  • Patients scheduled for CCTA examination

排除标准

  • Patients who did not complete the planned CT imaging procedure due to mechanical error of the CT machine.

结局指标

主要结局

CCTA utilization parameters and clinical findings

时间窗: Two years

次要结局

  • 90 day MACE, Intended Care Management and Cost Effectiveness for cardiologists interpreting their CCTA studies(Two years)

研究者

发起方
MDDX LLC
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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