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Improving Chronic Nocturnal Noninvasive Ventilation: a Multimodality Approach (NOCTIVENT)

U

University Medical Center Groningen (UMCG)

Status

Enrolling

Conditions

Chronic Respiratory Failure
Non-invasive Ventilation

Treatments

Device: Non-invasive ventilation

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

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.

Full description

Can be provided on request as the registry rules are no in Dutch

Enrollment

100 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

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

Trial design

100 participants in 1 patient group

COPD patients with Chronic Respiratory Failure
Treatment:
Device: Non-invasive ventilation

Trial contacts and locations

1

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Central trial contact

Marieke L Duiverman, MD PhD

Data sourced from clinicaltrials.gov

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