Actively Recruiting
External Validation of VVI
Led by University of Thessaly · Updated on 2026-02-11
100
Participants Needed
3
Research Sites
35 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Failure of liberation from mechanical ventilation increases days spent being mechanically ventilated, the length of stay and the morbidity of patients. Thus it is crucial that those patients who are ready to be liberated are accurately detected. In this study the investigators want to externally validate an index (the volume-velocity index, VVI) which in a preliminary study was found to predict with high accuracy the outcome of ventilator liberation. In this study, in patients who are deemed ready to undergo weaning by their treating physician the investigators will measure the excursion of the diaphragm, the principal respiratory muscle, the inspiratory time and the tidal volume and the volume breathed by the patient at each respiration in three phases: 1. during pressure support ventilation with 5/5, 2. during pressure support ventilation with 8/0, 3. during t-tube or pressure support ventilation with 0/0. All of these phases are ventilatory modalities widely used during weaning from mechanical ventilation. The investigators will evaluate whether VVI can predict accurately the weaning outcome.
CONDITIONS
Official Title
External Validation of VVI
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Mechanically ventilated patients for more than 48h
- First Spontaneous breathing trial
- Deemed as ready to undergo weaning by the treating physician, according to published readiness criteria (DOI: 10.1183/09031936.00010206)
You will not qualify if you...
- Pregnant patients
- Preexisting diaphragmatic disease or injury
- Tracheostomy
AI-Screening
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Trial Site Locations
Total: 3 locations
1
General University Hospital of Larissa
Larissa, Greece, 41110
Actively Recruiting
2
AHEPA - University General Hospital
Thessaloniki, Greece, 54636
Not Yet Recruiting
3
General Hospital of Thessaloniki "G. Papanikolaou"
Thessaloniki, Greece, 57010
Not Yet Recruiting
Research Team
A
Apostolos - Alkiviadis Menis, MD, PhD
CONTACT
D
Demosthenes Makris
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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