NCT00734045已完成不适用
Prospective Evaluation of the StatusFirst™ CHF NT-proBNP Device in Human Whole Blood and Plasma Samples
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 450
- 试验地点
- 2
- 主要终点
- StatusFirst CHF NT-proBNP test result
研究概览
简要总结
The primary objective of the study is to establish the correlation between NT-proBNP measurements in fresh human whole blood samples and those in plasma samples from the same study subjects, where said samples are collected in EDTA and Li-Hep anticoagulant tubes and measured by the StatusFirst™ CHF NT-proBNP device in conjunction with the DXpressTM Reader in a laboratory setting.
研究设计
- 研究类型
- Observational
- 时间视角
- Prospective
入排标准
- 年龄范围
- 45 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Have clinically confirmed heart failure (NYHA class I-IV) or have presented to an emergency room or clinic with signs, symptoms and/or risk factors suggestive of heart failure, OR
- •Be non-CHF controls greater than 45 years of age with no history of heart failure or cardiovascular disease.
排除标准
- •Be 45 years of age or younger
结局指标
主要结局
StatusFirst CHF NT-proBNP test result
时间窗: At presentation to study site (no follow-up)
次要结局
未报告次要终点
研究者
研究点 (2)
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