SaO2 Sampling
DeviceCO-Oximetry analysis of arterial blood samples
NCT Number: NCT06372106
The main goal of this study is to look at the performance of the neonatal, infant, and pediatric Philips SpO2 sensors with the Philips FAST Pulse Oximetry technology. Oxygen saturation measurements (SpO2) will be obtained via pulse oximetry and invasive arterial oxygen measurements (SaO2) will be obtained via arterial blood samples as part of your clinical care and assessed by co-oximetry. The study will aim to enroll a diverse population to help us understand the impact of skin pigmentation.
Interested in participating?
Request InfoAll sexes
Observational
Phoenix Children's, Phoenix, Arizona, United States
This is a prospective, multi-center, multi-phase, unblinded, non-randomized. self-controlled, observational study. All data analyses specified below will be calculated and summarized by each of SpO2 sensors under test. Demographics and baseline characteristics, including sex assigned at birth, age, ethnicity, race, baseline height, baseline weight, BMI, skin pigmentation and sensor application site measurements will be summarized with descriptive statistics using the analysis set.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CO-Oximetry analysis of arterial blood samples
Time frame: through study completion, an average of 8 months
The oximetry technology will be expressed in ARMS of SpO2 measurements obtained from neonatal, infant, and pediatric sensors with the Philips FAST Pulse Oximetry technology within the range of 70-100% in comparison to the SaO2 as ground truth.
Time frame: through study completion, an average of 8 months
Non-disparate bias with consideration to skin pigmentation for each neonatal, infant, and pediatric SpO2 sensor under test with the Philips FAST Pulse Oximetry technology.
Time frame: through study completion, an average of 8 months
Proportion of paired SaO2 and SpO2 readings in which occult hypoxemia (i.e., SaO2 <88% with SpO2 ≥92%) is identified among patients within the broad categories of light, medium, and dark pigmentation.
Contact information is provided by the study sponsor or research team.
Philips Clinical & Medical Affairs Global
Industry
Philips FAST picoSAT Convenience Sampling for Clinical Performance in Neonate, Infant, and Pediatric Patients
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06398262
Measurement, Nasal Alar Collapse, Bilateral
Stockholm, Sweden
View Trial DetailsNCT07223177
SpO2
Modesto, California, United States
View Trial DetailsNCT07404956
Abdominal Pain, Abdominal Pain (AP)
Bartın, Turkey (Türkiye)
View Trial DetailsNCT07615738
SpO2, SpO2 (Peripheral Oxygen Saturation) Measurement Validation
Omaha, Nebraska, United States
View Trial Details