Clinical Trials Directory

Trials / Terminated

TerminatedNCT04007146

Systematic Calculation of HyperOxygenation Transit Time

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

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
1 (actual)
Sponsor
University Hospital, Angers · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTTranscutaneous oxymetry measurementTranscutaneous oxymetry measurement with transient hyperoxia period (2 periods of 30seconds at 60% of oxygen)

Timeline

Start date
2020-03-01
Primary completion
2021-09-01
Completion
2021-09-01
First posted
2019-07-05
Last updated
2021-12-08

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04007146. Inclusion in this directory is not an endorsement.