Trials / Completed
CompletedNCT06484452
SpO2 Validation Study - Philips FAST 2024
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 113 (actual)
- Sponsor
- Philips Clinical & Medical Affairs Global · Industry
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
Validation study to compare the accuracy of non-invasive Philips SpO2 sensors in detecting blood oxygen levels compared to invasive methods requiring a blood draw and lab analysis.
Detailed description
To validate the SpO2 accuracy of the SpO2 sensors under test with the Philips FAST Pulse Oximetry technology during non-motion conditions over the range of 70-100% SaO2, when compared with the reference SaO2 obtained from CO-Oximetry analysis of arterial blood samples.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | No Intervention | No Intervention |
Timeline
- Start date
- 2024-05-06
- Primary completion
- 2024-08-29
- Completion
- 2024-08-29
- First posted
- 2024-07-03
- Last updated
- 2025-09-16
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06484452. Inclusion in this directory is not an endorsement.