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Clinical Trials/NCT02696018
NCT02696018
Completed
Not Applicable

Evaluation of Diaphragmatic Displacement During Spontaneous Breathing Trials in Critically Ill Patients

Università degli Studi di Ferrara1 site in 1 country44 target enrollmentJuly 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Università degli Studi di Ferrara
Enrollment
44
Locations
1
Primary Endpoint
Weaning success
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Acute respiratory failure (ARF) is characterised by a discrepancy between load imposed on respiratory muscles and their capacity. Recently, diaphragmatic ultrasonography has been introduced in the clinical practice to evaluate diaphragmatic function. In particular, the investigators will focus on Diaphragmatic Displacement measured by M-mode ultrasonography. The aim of this study was to compare the diaphragmatic displacement with traditional weaning parameters in potentially ready to be extubated patients undergoing a spontaneous breathing trial (SBT).

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
March 2015
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Università degli Studi di Ferrara
Responsible Party
Principal Investigator
Principal Investigator

Savino Spadaro

Dr

Università degli Studi di Ferrara

Eligibility Criteria

Inclusion Criteria

  • mechanically ventilated since more than 24 hours
  • clinical improvement of the underlying acute cause of the respiratory failure
  • adequate cough reflex
  • absence of excessive and/or purulent tracheobronchial secretion
  • stable cardiovascular status
  • stable metabolic status
  • adequate pulmonary function
  • adequate mentation

Exclusion Criteria

  • age \<18 years
  • pregnancy
  • presence of thoracostomy, pneumothorax or pneumomediastinum
  • presence of flail chest or rib fractures
  • neuromuscular disease
  • use of muscle-paralyzing agents within 48 hours before the study
  • history or new detection of paralysis or paradoxical movement of a single hemi-diaphragm on diaphragm ultrasonography

Outcomes

Primary Outcomes

Weaning success

Time Frame: within the first 48 hours after the spontaneous breathing trial

A successful weaning attempt was registered when patients were extubated and breathed spontaneously for more than 48 hours. The reinstitution of mechanical ventilation at the end of spontaneous breathing trial, reintubation within 48 hours or non-invasive ventilation (NIV) support after extubation defined a failed weaning attempt.

Study Sites (1)

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