NCT06633861

Data Collection Study for RFP (Respiration From Plethysmogram)

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 86 (actual)
• Sponsor: Philips Clinical & Medical Affairs Global · Industry
• Sex: All
• Age: 4 Years
• Healthy volunteers: Not accepted

Summary

The study will be conducted in hospitalised patients who undergo spot-check monitoring of vital signs as part of their routine care.

Detailed description

In an additional spot-check measurement procedure, the study will measure oxygen saturations through different Philips SpO2 finger sensors. Patients will wear a nasal cannula linked to a CO2 measuring device at the same time. The data from both devices will be used to design and improve algorithms for measurement of respiratory rate with the saturation probe and the Philips FAST pulse oximeter system. The study will include 50 adult patients and 25 pediatric patients.

Conditions

• In-patients Assessment of Vital Signs

Interventions

Type	Name	Description
DEVICE	spot-check measurement	Spot-check measurement: different Philips SpO2 sensors and Philips FAST pulse oximeter system, capnography

Timeline

• Start date: 2024-09-05
• Primary completion: 2024-11-07
• Completion: 2024-11-07
• First posted: 2024-10-09
• Last updated: 2025-09-16

Locations

1 site across 1 country: United Kingdom