SPO2 VALIDATION STUDY - PHILIPS FAST 2025
NCT07221526 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 86
Last updated 2026-04-01
Summary
Clinical investigation is to validate the SpO2 accuracy of the M1133AX5, M1133AX6, and AlarX4 (nasal ala application) SpO2 sensors under test with the Philips FAST Pulse Oximetry technology.
Conditions
- PULSE OXIMETRY
Interventions
- DEVICE
-
NO INTERVENTION
NO INTERVENTION
Sponsors & Collaborators
-
Philips Clinical & Medical Affairs Global
lead INDUSTRY
Principal Investigators
-
Monica Rabanal, NP · Element Desaturation Lab
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-10-28
- Primary Completion
- 2026-02-05
- Completion
- 2026-02-05
- FDA Device
- Yes
Countries
- United States
Study Locations
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