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Comprehensive Ultrasound Evaluation as a Predictor of Weaning

U

Università degli Studi di Ferrara

Status

Completed

Conditions

Weaning Failure
Mechanical Ventilation Weaning

Treatments

Diagnostic Test: Comprehensive evaluation

Study type

Observational

Funder types

Other

Identifiers

NCT05539599
WEAN_US

Details and patient eligibility

About

Several studies investigated the role of specific clinical predictors of weaning success, but it is determined by a combination of different aspects that can result in success or failure. Indeed, unresolved lung disease, cardiac dysfunction, loss of respiratory and core muscle strength can play a role in a failure weaning to mechanical ventilation (MV). The investigators hypothesized that a combined score that include heart, lung, and respiratory muscle ultrasound (US) evaluation could be able to predict the ability of weaning success. Furthermore, it will be described weather the days of MV before weaning trial may affect the relevance of each clinical variable evaluated.

Full description

Critically ill patients undergone at least 48 hours of MV and ready to spontaneous breathing trial (SBT) will be included in the study. The spontaneous breathing trial is performed in pressure support ventilation with a clinician-set positive end expiratory pressure (PEEP) ≤ 5 cm H2O and FiO2< 40%. In addition to the parameters traditionally used for the evaluation of weaning (RSBI), the investigators will perform ultrasound evaluation of diaphragm, lung parenchyma, cardiac function, and the strength of the hand grip.

Investigators will evaluate the diaphragmatic parameters (thickening fraction,TF, and diaphragmatic displacement, DD) and TFmax (TF during forced breathing /TF during tidal respiration) to identify the inspiratory reserve. Weaning success is considered as liberation from MV within 72 hours.

Enrollment

89 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged between 18 and 90 years
  • Mechanical ventilation> 48 h
  • Reason for ICU admission: medical / surgical / trauma

Exclusion criteria

  • age under 18
  • diagnosis of neuromuscular disease
  • tracheostomy
  • terminal extubation
  • pregnancy in progress -
  • previous paralysis of the diaphragm or of a hemidiaphragm
  • use of neuromuscular blocking drugs in continuous infusion in the 48 hours preceding the weaning attempt.
  • Refusal to participate in the study

Trial design

89 participants in 1 patient group

Cohort
Description:
Patients will undergo a spontaneous breathing trial. Any extubation will be decided by an independent operator.
Treatment:
Diagnostic Test: Comprehensive evaluation

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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