Pulse oximeters in Paediatric Patients
- Conditions
- Cardiac surgeryAnaesthesiology - AnaestheticsCardiovascular - Other cardiovascular diseases
- Registration Number
- ACTRN12621001330831
- Lead Sponsor
- The Royal Children's Hospital Melbourne
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
•Under the age of eighteen years old
•Undergoing cardiac surgery requiring placement of an arterial line for routine clinical care at RCH or who have congenital heart disease and are in the intensive care unit at RCH with an arterial line for routine clinical management
•Has a legally acceptable representative capable of understanding the study information sheet and providing verbal consent on the participant’s behalf
•Completes the patient demographic/characteristic survey or has a legally acceptable representative capable of understanding the survey who completes it on the participant’s behalf
•Is classified as not having pulsatile peripheral flow, as in the setting of a ventricular assist device
Participants may also be excluded if they have previously participated in this study, pending enrolment numbers.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Accuracy compared to standard pulse oximeter.<br><br>Accuracy will be determined by using comparison of oxygen saturation measured by study pulse oximeter compared to oxygen saturation measured by standard pulse oximeter,[ At the time of drawing the usual baseline arterial blood gas, after the study pulse oximeter has been placed on the patient and allowed to reach a plateau after fifteen seconds.<br>];Accuracy compared to co-oximetry measurements.<br><br>Accuracy willl be determined using comparison of oxygen saturation from arterial blood gas measurements with study pulse oximeter readings.[ At the time of drawing the usual baseline arterial blood gas, after the study pulse oximeter has been placed on the patient and allowed to reach a plateau after fifteen seconds.<br>]
- Secondary Outcome Measures
Name Time Method