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Variability of SpO2 Measurements Depending on the Choice of Finger for Sensor Placement — FinSpO2  

Hypoxia Clinical Trial

Official title:
Variability of SpO2 Measurements Depending on the Choice of Finger for Sensor Placement

Clinical Trial Summary

The aim of the project is to experimentally determine the effect of the choice of finger for the placement of a pulse oximeter sensor on the results of measuring peripheral blood oxygen saturation (SpO2) in a healthy person with short-term hypoxia and hypercapnia.

Clinical Trial Description

The aim of the project is to experimentally determine the effect of the choice of finger for the placement of a pulse oximeter sensor on the results of measuring peripheral blood oxygen saturation (SpO2) in a healthy person with short-term hypoxia and hypercapnia. This is an intervention prospective study that will take place at the Faculty of Biomedical Engineering, especially on FBMI students. The experiment consists of two phases, in which in the first phase, the volunteers will inhale the hypoxic mixture for five minutes after the stabilization phase. In the second phase, volunteers inhale a hypoxic and hypercapnic mixture. During the experiment, non-invasive SpO2 measurements will be performed continuously on individual fingers of both volunteer hands. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04771663
Study type Interventional
Source Czech Technical University in Prague
Contact
Status Enrolling by invitation
Phase N/A
Start date January 10, 2021
Completion date October 15, 2023
View Details
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