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Weaning Algorithm for Mechanical VEntilation

NCT03697785 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 286

Last updated 2018-10-05

No results posted yet for this study

Summary

To compare the duration of mechanical ventilation and the weaning period between two groups of patients managed with either Standard Care or with mechanical ventilation adjusted according to the Beacon Caresystem, in patients receiving mechanical ventilation for more than 24 hours

Conditions

  • Respiration, Artificial
  • Critical Care
  • Respiratory Insufficiency
  • Intensive Care (ICU) Myopathy
  • Mechanical Ventilation Complication

Interventions

DEVICE

Beacon Care System

Beacon has been developed by Mermaid Care in Denmark. BEACON is a critical care ventilation assist system (http://beaconcaresystem.com/beacon-5/), which potentially enables better ventilation strategies and a more efficient patient care workflow. As an add-on to standard ventilation systems it provides ventilation recommendations 24/7 based on non-stop, personalised monitoring/diagnostics of patients. Based on unique mathematical algorithms and physiological models, it recommends changes in ventilation settings, supporting the critical decision-making processes.

Sponsors & Collaborators

  • Mermaid Care A/S

    collaborator UNKNOWN

  • Aalborg University

    collaborator OTHER

  • Imperial College London

    collaborator OTHER

  • Royal Brompton & Harefield NHS Foundation Trust

    lead OTHER

Principal Investigators

  • Brijesh Patel, MBBS PhD · Royal Brompton & Harefield NHS Foundation Trust

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-24
Primary Completion
2021-10-01
Completion
2021-10-01

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 NCT03697785 on ClinicalTrials.gov