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PRICO: OPTI Target Range — POSTR  

Very Low Birth Weight Infant Clinical Trial

Official title:
Evaluation of the Impact of a Narrower SpO2 Target Range on Performance of an Automatic FiO2 Control System: a Randomized Study

Clinical Trial Summary

The aim of the study is to determine if a narrower SpO2 Target Range setting automated control of FiO2 (A-FiO2) is more effective than a wider SpO2 Target Range

Clinical Trial Description

A-FiO2 systems have consistently proven to be more effective than manual control. Because it is more precise than manual control, studies of some A-FiO2 systems found small differences in the set target range (shift in the median and width) can optimize the relative performance. Similar studies of the A-FiO2 system (PRICO) used in the investigator's NICU have not been conducted. The standard of practice in the investigator's NICU is to use 4 different target ranges to balance the risk of hypoxia and hyperoxia based on the gestational age vulnerabilities. Based on the studies of other A-FiO2 systems the investigators believe a slightly narrower width target range would be more effective. Therefore, a small systematic study is needed to determine the optimal set target range to achieve the therapeutic goal. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06207994
Study type Interventional
Source Czech Technical University in Prague
Contact Jakub Rafl, PhD
Phone +420728229991
Email rafl@fbmi.cvut.cz
Status Recruiting
Phase N/A
Start date February 20, 2024
Completion date October 2024
View Details
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