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临床试验/NCT03685097
NCT03685097已完成不适用

Comparison of Two Point-of-care Devices for Viscoelastic Hemostasis Assays

HemoSonics LLC1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年3月1日最近更新:
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 QPlus Clot Time and Clot Stiffness results to comparable ROTEM delta results

研究概览

简要总结

This study will investigate the correlation and agreement of Quantra-derived parameters with parameters reported by the ROTEM delta and standard laboratory tests in cardiac surgery patients. In addition the association of Quantra-derived parameters with select platelet function tests will be investigated.

详细描述

The Quantra System is a fully integrated and automated in vitro diagnostic device which uses SEER Sonorheometry, an ultrasound-based technology, to characterize the viscoelastic properties of a whole blood sample during coagulation. The Quantra QPlus Cartridge (previously called the Surgical Cartridge), was developed to monitor hemostasis during major surgical procedures in adult patients. The cartridge provides six parameters that depict the functional status of a patient's coagulation system.

This single site, prospective observational study will investigate the correlation and agreement of Quantra-derived parameters with parameters reported by the ROTEM delta and standard laboratory tests (PT, aPTT, fibrinogen, platelet count) in cardiac surgery patients. As an additional exploratory study, the association of Quantra-derived parameters with select platelet function tests will be investigated.

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 >18 years
  • Subject is undergoing elective cardiac surgery with cardiopulmonary bypass
  • Subject is willing to participate and has signed a consent form

排除标准

  • Subject is younger than 18 years
  • Subject has known congenital coagulopathy
  • Subject is unable to provide written informed consent

结局指标

主要结局

Comparison of QPlus Clot Time and Clot Stiffness results to comparable ROTEM delta results

时间窗: Baseline (before surgery)

Coagulation function assessed by Quantra QPlus Cartridge and ROTEM delta

Comparison of QPlus Clot Time and Clot Stiffness results to comparable ROTEM delta

时间窗: After cardiac bypass (10 minutes after administration of protamine)

Coagulation function assessed by Quantra QPlus Cartridge and ROTEM delta

Comparison of QPlus Clot Time and Clot Stiffness results to standard coagulation test results

时间窗: After cardiac bypass (10 minutes after administration of protamine)

Coagulation function assessed by Quantra QPlus Cartridge and standard coagulation tests

次要结局

  • Comparison of QPlus Clot Stiffness results to platelet function tests with multiple electrode aggregometry (MEA): ADPtest and TRAPtest(After cardiac bypass (10 minutes after administration of protamine))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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