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Philps FAST2022 picoSAT Pulse Oximetry Desaturation Study

NCT05683366 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 72

Last updated 2024-04-03

No results posted yet for this study

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.

Conditions

  • SpO2 (Peripheral Oxygen Saturation) Measurement Validation

Interventions

DEVICE

No Intervention

There is no intervention in this study

Sponsors & Collaborators

  • Philips Clinical & Medical Affairs Global

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-12-13
Primary Completion
2023-09-07
Completion
2023-09-07
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05683366 on ClinicalTrials.gov