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RECRUITING
NCT07223177
NA

Philips FAST SpO2 Technology With Masimo Sensors for SpO2 Monitoring in the Neonatal, Infant, and Pediatric Populations

Sponsor: Masimo Corporation

View on ClinicalTrials.gov

Summary

The objective of this study is to verify the form, fit and function of the Philips FAST technology with Masimo neonatal, infant and pediatric sensors for SpO2 monitoring in the respective indicated populations. The study design uses convenience sample data collection from neonatal, infant, and pediatric sensors within their respective indicated patient populations that have a range of different skin pigmentations, simultaneously with an FDA cleared pulse oximeter as a comparator.

Key Details

Gender

All

Age Range

0 Years - 21 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2025-12-17

Completion Date

2026-06-05

Last Updated

2026-03-04

Healthy Volunteers

Yes

Conditions

Interventions

DEVICE

Masimo Sensor (RD SET and/or LNCS) connected to Philips Monitor using Philips FAST SpO2 Algorithm

Subjects may use multiple Masimo sensors (RD SET and/or LNCS). All subjects will have at least one Masimo sensor (RD SET or LNCS) connected to Philips Monitors using Philips FAST SpO2 Algorithm

Locations (2)

Paradigm Clinical Research

Modesto, California, United States

Paradigm Clinical Research

San Diego, California, United States