NCT07168213View on ClinicalTrials.gov

Comparison of Two SpO2 Targets With Two Different Oximeters - Impact on FiO2 During Nasal High Flow Oxygen Therapy

NANot yet recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

October 31, 2025

Primary Completion Date

June 30, 2027

Study Completion Date

December 31, 2027

Conditions
Oxygen DeliveryAcute Respiratory FailureHigh Flow Oxygen TherapyHypoxemic Acute Respiratory Failure
Interventions
DEVICE

Manual FiO2 titration with Philips oximeter (SpO2 target 90%)

FiO2 titration to reach the SpO2 target (set at 90%) with Philips oximeter

DEVICE

Manual FiO2 titration with Nonin oximeter (SpO2 target 90%)

FiO2 titration to reach the SpO2 target (set at 90%) with Nonin oximeter

DEVICE

Manual FiO2 titration with Philips oximeter (SpO2 target 94%)

FiO2 titration to reach the SpO2 target (set at 94%) with Philips oximeter

DEVICE

Manual FiO2 titration with Nonin oximeter (SpO2 target 94%)

FiO2 titration to reach the SpO2 target (set at 94%) with Nonin oximeter

Trial Locations (1)

G1V4G5

Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval, Québec

All Listed Sponsors
lead

Laval University

OTHER

NCT07168213 - Comparison of Two SpO2 Targets With Two Different Oximeters - Impact on FiO2 During Nasal High Flow Oxygen Therapy | Biotech Hunter | Biotech Hunter