Actively Recruiting

Age: 18Years +
All Genders
NCT07372664

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

You will not qualify if you...

  • Pregnant patients
  • Preexisting diaphragmatic disease or injury
  • Tracheostomy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

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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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