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 type | Observational |
|---|---|
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | University Medical Center Groningen Academic / other |
| Locations | 1 site (Groningen) |
| Status | Recruiting |
| Started | December 1, 2024 |
| Main results expected | December 1, 2028 |
| Study ends | December 1, 2028 |
| Registry record updated | July 2, 2026 |
| Trial ID | NCT05756387 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.
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Early Non-Invasive Ventilation in ALS
This study tests whether starting non-invasive ventilation earlier in adults with ALS can help improve breathing and quality of life.
-
Turkish version of the S3-NIV questionnaire: testing its reliability for home NIV patients
We’re testing whether the Turkish S3-NIV questionnaire reliably measures how well patients on home non-invasive ventilation can manage daily use and comfort.
-
Extra oxygen during the 6-minute walk for people with chronic respiratory failure or exercise-related low oxygen
This trial will test whether giving extra oxygen during a 6-minute walk helps people with chronic respiratory failure or exertional low oxygen from COPD or interstitial lung disease walk farther, breathe better, and feel easier during the test.
-
Machine learning to detect inspiratory leak in long-term non-invasive ventilation
This project tries to use a machine-learning program to detect inspiratory leaks in people with chronic respiratory failure who use long-term non-invasive ventilation.
-
Monitoring breathing muscle function in ARF patients on non-invasive support
This study tests whether advanced breathing-muscle monitoring can help care teams manage adults with acute respiratory failure who are on non-invasive respiratory support.
-
Home oxygen with high-flow therapy vs standard oxygen for chronic lung and heart disease
In people with long-term lung or heart conditions who need oxygen after leaving the hospital, the study tests whether a high-flow nasal cannula (HFNC) can improve breathing comfort and quality of life compared with standard oxygen therapy.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.