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NCT07449715 · ClinicalTrials.gov registry record
Respiration From Pleth Validation
A clinical trial of Respiratory Rate Monitoring, sponsored by Philips Clinical & Medical Affairs Global.
- Recruiting
- Registry status
- 113
- Enrollment target
- 2
- Study locations
NCT07449715: Recruiting study of Respiratory Rate Monitoring, sponsored by Philips Clinical & Medical Affairs Global.
NCT07449715 is a study of Respiratory Rate Monitoring that is actively recruiting participants, run by Philips Clinical & Medical Affairs Global. The registered enrollment target is 113 participants. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07449715, a study of Respiratory Rate Monitoring, is actively recruiting participants, sponsored by Philips Clinical & Medical Affairs Global.
- RECRUITING
- Registry status
- 113 participants
- Enrollment target
- 2
- Study locations
Study 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.
Primary Outcome
Accuracy Root Mean Square (ARMS) between respiratory rate derived from plethysmography using Philips FAST Pulse Oximetry technology and respiratory rate derived from clinician-annotated capnography waveforms. Metric: ARMS (breaths per minute). Pass/Fail Criterion: ARMS ≤ 3 BPM per population (adult, pediatric).
Conditions Studied
Interventions
- DEVICE Physiological Monitoring with SpO₂ Sensors and Capnography
Study Locations (2)
North Carolina
- Duke University Hospital - Durham
Gwynedd
- Ysbyty Gwynedd - Bangor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 113 participants |
| Start Date | 2026-02-06 |
| Est. Completion | 2026-05-25 |
What NCT07449715 shows while recruiting
NCT07449715 is an observational study that tracks outcomes without assigning an intervention. The registered 113 participants enrollment target is mid-sized for trials with a published cap.
The record links to 1 condition, with Respiratory Rate Monitoring appearing as the primary indexed condition, and to 1 intervention - of which Physiological Monitoring with SpO₂ Sensors and Capnography is the first listed.
NCT07449715 reports a single indexed study location in North Carolina, Gwynedd.
Frequently Asked Questions
What is clinical trial NCT07449715 about?
NCT07449715 is a clinical study titled "Respiration From Pleth Validation". 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-appro...
What is the current status of trial NCT07449715?
This trial is currently recruiting. The enrollment target is 113 participants. The study started on 2026-02-06. Estimated completion is 2026-05-25.
What conditions does trial NCT07449715 study?
This clinical trial studies the following conditions: Respiratory Rate Monitoring.
What interventions are being tested in trial NCT07449715?
The interventions under investigation include: Physiological Monitoring with SpO₂ Sensors and Capnography (DEVICE).
Who is sponsoring clinical trial NCT07449715?
This trial is sponsored by Philips Clinical & Medical Affairs Global, which has 45 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07449715 being conducted?
This trial has 2 study locations across North Carolina, Gwynedd. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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