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临床试验/NCT03705299
NCT03705299已完成不适用

A Prospective, Comparative Study to Evaluate the Accuracy of a Non-Invasive Central Venous Pressure Method to the Standard CVP Method

The Cooper Health System0 个研究点目标入组 40 人开始时间: 2012年11月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
主要终点
Assessing if the NeuMeDx NICVP device is as effective as the standard invasive method at measuring CVP in patients that require central catheter placement and monitoring.

研究概览

简要总结

This is a prospective, comparative, internally controlled device study that will enroll a total of 100 adult patients that require the placement of central venous catheter and CVP monitoring to assess volume status and cardiac preload.

详细描述

Standard CVP Method

The CVP line is inserted into the internal jugular vein central venous catheter or subclavian vein catheter and threaded to the point where the superior vena cava meets the inferior vena cava prior to entry into the right atrium of the heart. The catheter is hooked to a pressure bag which is pressurized to 200 cm water. This pressure allows the infusion of about 3ml of fluid each hour but keeps the line patent. The distal tip of the CVP line is connected to a transducer and taped to the arm at a level which is in line with the heart.

Research Procedure (non-invasive CVP Method)

A physiologic data acquisition system (Zoe Medical, Topsfield MA)) will be used to monitor CVP, upper arm impedance changes, and upper arm cuff pressures.

The subject's CVP pressure transducer will be zeroed at the level of the right atrium (midaxillary line) with the use of a carpenter's level.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

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

  • Patients aged ≥ 18 years
  • Require CVP monitoring in the supine position as part of routine care
  • Central venous access obtained by either internal or external jugular, or subclavian vein

排除标准

  • Patients aged < 18 years
  • Patients who are pregnant
  • Patients that will be in the prone position
  • Central venous access obtained by the femoral vein

研究组 & 干预措施

NeuMeDex NICVP (Non-Invasive CVP) vs Standard CVP

Experimental

Three pressure readings recorded for both NeuMeDex NICVP and central line pressure catheter over a 10 minute period.

干预措施: Non-Invasive CVP vs Standard CVP (Device)

结局指标

主要结局

Assessing if the NeuMeDx NICVP device is as effective as the standard invasive method at measuring CVP in patients that require central catheter placement and monitoring.

时间窗: 6 months

The primary objective of the study is to measure the CVP using the NeuMeDx NICVP (Non-Invasive Central Venous Pressure) device. The critical endpoint is the average of the average of three CVP, by calibrated forced transducer, and NICVP measurements in mmHg over a 10-minute period in a patient in the supine position.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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