Clinical trial Recruiting at 1 site Observational

Improving home ventilation for chronic respiratory failure patients

Official title: Improving Chronic Nocturnal Noninvasive Ventilation: a Multimodality Approach

Run by University Medical Center Groningen · NCT05756387 · Data updated 2026-11-12

This study is testing a new way to monitor patients with chronic respiratory failure who use home ventilation to see if it improves their breathing comfort and effectiveness.

Quick facts

Study typeObservational
SexAll
Enrollment100 (estimated)
SponsorUniversity Medical Center Groningen
Academic / other
Locations1 site (Groningen)
StatusRecruiting
StartedDecember 1, 2024
Main results expectedDecember 1, 2028
Study endsDecember 1, 2028
Registry record updatedJuly 2, 2026
Trial IDNCT05756387 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are COPD patients who require chronic home non-invasive ventilation.

Probably not a fit

Patients who are unable to read the consent form or cannot perform measurements at home may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to develop a reliable method for remotely monitoring patients on chronic home non-invasive ventilation (NIV). It will assess ventilatory efficacy and patient comfort by collecting data on gas exchange, lung mechanics, and patient-ventilator interaction. The study will create a databank of synchronously acquired datasets from standard care monitored parameters and newly acquired non-invasive data on patient effort and lung inflation during NIV setup and follow-up.

Why it matters

Potential benefit: If successful, this approach could enhance the management of chronic respiratory failure, leading to improved patient outcomes and comfort.

How similar studies have gone: Other studies have shown promise in improving patient outcomes with similar monitoring approaches, indicating potential for success in this study.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* COPD patients indicated for chronic home NIV

Exclusion Criteria:

* not able to read the written information and/or sign the informed consent form
* no possibility to perfrom measurements at home

Where it's running

  • Umcg
    Groningen, Netherlands
    Recruiting

Study contacts

  • Principal investigator: Marieke L Duiverman — University Medical Center Groningen
  • Study coordinator: Marieke L Duiverman, MD PhD
  • Email: m.l.duiverman@umcg.nl
  • Phone: 0031503613200

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.