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Improving Chronic Nocturnal Noninvasive Ventilation: a Multimodality Approach

NCT05756387 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2024-12-13

No results posted yet for this study

Summary

The aim of the data collection is to create an advanced reliable method to remotely monitor patient on chronic home non-invasive ventilation (NIV), both regarding ventilatory efficacy and patient comfort, both in the hospital and at home by assessing gas exchange, lung mechanics and the interaction between the patient and the ventilator.

For this purpose, we will set-up of databank of synchronously acquired datasets of already standard care monitored parameters during NIV (transcutaneous monitoring of gas exchange; ventilator data including data on PVA), and newly non-invasively acquired data on patient effort (EMG, patient ratings) and lung (hyper)inflation (EIT), during the set-up and follow-up of standard care chronic NIV.

Conditions

  • Chronic Respiratory Failure
  • Non-invasive Ventilation

Interventions

DEVICE

Non-invasive ventilation

NIV as in standard care

Sponsors & Collaborators

  • University of Twente

    collaborator OTHER

  • Löwenstein BV

    collaborator UNKNOWN

  • Vivisol

    collaborator OTHER

  • Sencure BV

    collaborator UNKNOWN

  • University Medical Center Groningen

    lead OTHER

Principal Investigators

  • Marieke L Duiverman · University Medical Center Groningen

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-01
Primary Completion
2028-12-01
Completion
2028-12-01
FDA Device
Yes

Countries

  • 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 NCT05756387 on ClinicalTrials.gov