Clinical Trial

Respiration From Pleth Validation

Study acronym: RfP Validation
Recruiting
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Record status
This record was last updated March 4, 2026 (before its estimated May 25, 2026 completion). Its status may not reflect the trial's current state.
Summary
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.
Trial Details
NCT Number NCT07449715
Lead Sponsor Philips Clinical & Medical Affairs Global
Conditions Respiratory Rate Monitoring
Enrollment 113 participants
Start Date 2026-02-06
Primary Completion 2026-05-25 (estimated)
Study Completion 2026-05-25 (estimated)
Updated on ClinicalTrials.gov 2026-03-04