Condition: Respiratory Rate Monitoring · Sponsor: Philips Clinical & Medical Affairs Global
This observational clinical investigation evaluates the performance of respiratory rate derived from the plethysmography waveform (Respiration from Pleth, RfP) using Philips FAST Pulse Oximetry technology. Adult and pediatric inpatients will undergo noninvasive monitoring using age- and weight-appropriate SpO₂ sensors and capnography, with capnography serving as the reference standard. The study assesses accuracy, mean bias, precision, and time to first valid respiratory-rate value across continuous and spot-check conditions. No device outputs are used for clinical decision-making, and all procedures occur during a single study visit.
This description comes directly from the study's public registry record.
Nero Evero, Clinical Study Manager, MS · +1 720-201-7689 · nero.evero@philips.com
Always discuss trial participation with your own doctor first.
| Duke University Hospital | Durham, North Carolina, United States | Recruiting |
| Ysbyty Gwynedd | Bangor, Gwynedd, United Kingdom | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT07449715