跳至主要内容
临床试验/NCT04007146
NCT04007146终止不适用

Systematic Calculation of HyperOxygenation Transit Time Mesure transcutanée de l'oxygène au Cours de l'Hyperoxie Transitoire

University Hospital, Angers1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2020年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
1
试验地点
1
主要终点
Estimation of transcutaneous oxymetry with transient hyperoxia

研究概览

简要总结

Cardiac output (CO) is an essential physiological parameter of healthy person or illness.

In clinical practices, all methods of measuring the CO(Fick method, thoracic impedance, esophageal echodoppler etc) contain limit. Each method are dangerous or hard to implement.

CO is probably determining element of blood transit time and thus the availability of oxygen between the central organs (heart, lung) and the peripheral organs (leg, arms).

Our hypothesis is transcutaneous oxymetry mesurement with oxygen inhalation, to cause a transient hyperoxia, can be used to determinate blood transit time between central organs and peripheral organs. This simple method will be non invasive technique.

详细描述

At admission eligible patients are proposed to participate. Written consent is signed after complete oral and written explanation of the protocol is signed.

The time of onset hyperoxia will be compare to usual CO method by cross correlation.

The duration of participation for subject is equal to 1 hour.

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
是

入选标准

  • •Adults over 18
  • •Cardiac output measurement considered at least 2 hours prior to the study
  • •Affiliation to a French National healthcare system
  • •Written informed consent must be obtained prior to protocol-specific

排除标准

  • •Acute or decompensated cardiac or respiratory failure
  • •Allergy to medical adhesives
  • •Patients under reinforced protection, pregnancy, deprived of liberty by judicial or administrative decision, hospitalized without consent or admitted to a health or social establishment for purposes other than research
  • •Inability to understand the instructions or objectives of the study

研究组 & 干预措施

Cardiac Output Measurement

Experimental

Subject will have a usual cardiac output

干预措施: Transcutaneous oxymetry measurement (Diagnostic Test)

结局指标

主要结局

Estimation of transcutaneous oxymetry with transient hyperoxia

时间窗: 24 months

Transition time calcutation from oxygen to peripheral organs by transcutaneous oxymetry method.

Average of CO measured

时间窗: 24 months

Average of CO by usual method (catheterisation or transoesophageal echocardiography) reported in medical record of patients

次要结局

未报告次要终点

研究者

发起方
University Hospital, Angers
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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