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An InnovaTive Approach to Ventilator-Induced Diaphragmatic Dysfunction

An InnovaTive Approach to Ventilator-Induced Diaphragmatic Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02299986
Acronym
ITAVIDD
Enrollment
56
Registered
2014-11-24
Start date
2013-04-30
Completion date
2015-06-30
Last updated
2015-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventilator-induced Diaphragm Dysfunction, VIDD

Brief summary

'Ventilator-Induced Diaphragmatic Dysfunction (VIDD) was originally described by Vassilakopoulos and Petrof in 1998, where it is used to cover the effects of mechanical ventilation and respiratory muscle unloading on the diaphragm. A recent article by Grosu and colleagues has demonstrated that the thickness of the diaphragm decreases with about 6% a day in a small cohort of mechanically ventilated patients. This is a longitudinal, single-centre, observational cohort study to examine the long-term effects of invasive mechanical ventilation on the diaphragm, and to study the risk factors associated with VIDD.

Interventions

Thickness measurement through ultrasound. The investigators will perform daily ultrasound measurements to assess the evolution in thickness during mechanical ventilation

Sponsors

University Hospital, Antwerp
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The patient must suffer from respiratory insufficiency requiring mechanical ventilation

Exclusion criteria

* The patient has been hospitalized and mechanically ventilated (invasive or non- invasive) in the period up to 1 year before start of the study. * The patient is known or suspected to have an anatomical malformation of the diaphragm. * The patient suffers from a disease that may impair diaphragmatic function: * Central neural disease at the level of the brain (Multiple sclerosis, stroke, Arnold-Chiari malformation) and spinal cord (quadriplegia, amyotrophic lateral sclerosis, poliomyelitis, spinal muscular atrophy, syringomyelia). * Neural disease of the phrenic nerve (Guillain-Barré syndrome, tumor compression, neuralgic neuropathy, chronic inflammatory demyelinating polyneuropathy, Charcot-Marie-Tooth disease). * Disorders of the neuromuscular junction (Myasthenia gravis, Lambert- Eaton syndrome, botulism, organophosphate poisoning). * Muscular diseases (muscular dystrophies, myositis (infectious, inflammatory, metabolic). * The patient is known or suspected to have a psychiatric illness inhibiting his/her cooperation with the study protocol or possibly obscuring the obtained results. * The patient has been mechanically ventilated for over 24 hours before the first ultrasonographic measurement can be performed.

Design outcomes

Primary

MeasureTime frame
Change in diaphragm thicknessParticipants will be followed during their ICU stay, an expected average of 1 week

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026