The New Golden Standard: the Early Warning Score Algorithm

NCT04292158 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2020-05-15

No results posted yet for this study

Summary

The objective is this study is the development and implementation of a smart algorithm to compute an early warning indicator able to predict early patient deterioration.

Conditions

  • Early Warning Score

Interventions

DEVICE

SomnoTouch

The patient will be equipped with the SomnoTouch device. This device is able to record and estimate the following data: ECG data PPG data Heart rate Respiration rate Blood pressure (mmHg) Oxygen saturation (%). All patient will be stored for further analysis.

DEVICE

MOX

The patient will be equipped with the MOX device. This device is able to record and estimate the following data: Accelerometers data Activity Body posture All patient will be stored for further analysis.

Sponsors & Collaborators

  • Academisch Ziekenhuis Maastricht

    collaborator OTHER
  • KU Leuven

    collaborator OTHER
  • Ziekenhuis Oost-Limburg

    collaborator OTHER
  • Hasselt University

    collaborator OTHER
  • Maastricht University

    collaborator OTHER
  • University of Liege

    lead OTHER

Principal Investigators

  • Patrizio Lancellotti · Liège University Hospital - CHU de Liège

  • Pierre Delanaye · Liège University Hospital - CHU de Liège

  • Arnaud Ancion · Liège University Hospital - CHU de Liège

  • Pieter Vandervoort · Department of Cardiology and Department Future Health, Ziekenhuis Oost-Limburg

  • Dianne de Korte-de Boer · Maastricht University Medical Centre, department of Anesthesiology

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-04-01
Primary Completion
2019-11-04
Completion
2020-04-30

Countries

  • Belgium
  • Netherlands

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 NCT04292158 on ClinicalTrials.gov