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临床试验/NCT02978872
NCT02978872已完成不适用

Comparison of Coagulation Parameters in Arterial and Venous Blood Measured Using the Quantra System

HemoSonics LLC1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2016年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
Comparison of Clot Time and Clot Stiffness results between arterial and venous samples

研究概览

简要总结

The Quantra™ System is a novel point-of-care diagnostic device designed to perform whole blood coagulation analysis. This study compares Quantra measurements determined in arterial versus venous blood samples obtained from patients undergoing cardiac surgery.

详细描述

The Quantra System is a fully integrated and automated in vitro diagnostic device which utilizes SEER Sonorheometry, an ultrasound-based technology, to characterize the dynamic changes in the viscoelastic properties of a blood sample during coagulation and clot lysis. Viscoelastic testing performed using existing technologies is typically performed on arterial samples obtained from patients undergoing surgical procedures, although reference ranges for these tests have been established for venous blood only.

The aim of this study is to evaluate potential differences between Quantra measurements determined in arterial versus venous blood samples obtained from patients undergoing cardiac surgery.

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

  • Subject is scheduled for cardiac surgery, utilizing cardiopulmonary bypass, or including placement of a ventricular assist device
  • Subject is ≥18 years
  • Subject is willing to participate and he/she has signed a consent form
  • Subject may participate if they have a history of bleeding or are on preoperative anticoagulant therapy

排除标准

  • Subject is unable to provide written informed consent
  • Subject is younger than 18 years
  • Subject is incarcerated at the time of the study
  • Subject is currently enrolled in a study that may confound the results of the proposed study
  • Subject is affected by a condition that, in the opinion of the surgical team, may pose additional risks

结局指标

主要结局

Comparison of Clot Time and Clot Stiffness results between arterial and venous samples

时间窗: Up to 24 hours

Coagulation function assessed by Quantra at 2 time points (Baseline and either during cardiac bypass or post-bypass)

次要结局

  • Comparison of Quantra results to comparable ROTEM results in venous samples(Up to 24 hours)
  • Comparison of Quantra results to standard coagulation test results in venous samples(Up to 24 hours)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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