Actively Recruiting

All Genders
NCT05756387

Improving Chronic Nocturnal Noninvasive Ventilation: a Multimodality Approach

Led by University Medical Center Groningen · Updated on 2024-12-13

100

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

Sponsors

U

University Medical Center Groningen

Lead Sponsor

U

University of Twente

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

Improving Chronic Nocturnal Noninvasive Ventilation: a Multimodality Approach

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • COPD patients indicated for chronic home NIV
Not Eligible

You will not qualify if you...

  • Unable to read the written information or sign the informed consent form
  • No possibility to perform measurements at home

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UMCG

Groningen, Netherlands

Actively Recruiting

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Research Team

M

Marieke L Duiverman, MD PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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