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Data Collection Study for RFP (Respiration From Plethysmogram)

NCT06633861 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2025-09-16

No results posted yet for this study

Summary

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

Conditions

  • In-patients Assessment of Vital Signs

Interventions

DEVICE

spot-check measurement

Spot-check measurement: different Philips SpO2 sensors and Philips FAST pulse oximeter system, capnography

Sponsors & Collaborators

  • Betsi Cadwaladr University Health Board

    collaborator OTHER_GOV

  • Philips Clinical & Medical Affairs Global

    lead INDUSTRY

Principal Investigators

  • Christian P Subbe, Dr. · Betsi Cadwaladr University Local Health Board

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
4 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-05
Primary Completion
2024-11-07
Completion
2024-11-07

Countries

  • United Kingdom

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 NCT06633861 on ClinicalTrials.gov