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Clinical Trials/NCT05763134
NCT05763134
Completed
Not Applicable

Critical Care Ultrasound Guided Weaning

Antalya Training and Research Hospital1 site in 1 country27 target enrollmentMarch 1, 2023
ConditionsWeaning Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Weaning Failure
Sponsor
Antalya Training and Research Hospital
Enrollment
27
Locations
1
Primary Endpoint
Mechanical ventilation weaning success
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Weaning patients from the ventilator in the intensive care unit is sometimes difficult because of three main interrelated etiologies: impaired lung, heart or diaphragm function. In this context, ultrasonography performed during tests for extubation of patients may enable the diagnosis of cardiac dysfunction, loss of pulmonary aeration, diaphragm dysfunction, and venous congestion, thereby reducing the number of failures in extubation.

The combination of TTE (Trans Thoracic Echocardiography), LUS (Lung Ultrasound), DUS (Diaphragmatic ultrasound) and VEXUS (Venous excess Ultrasound) may enable the identification of the etiology of weaning failure and reduce the number of extubation failures by enabling the development of an appropriate treatment strategy. With this study, it is aimed to contribute to the literature in this sense.

Detailed Description

The aim of this study is to reduce the number of extubation failures by defining the etiology of weaning failure and developing appropriate treatment strategies by using intensive care ultrasonography applications in combination (defining cardiac, pulmonary, diaphragmatic and venous congestion). Most patients can be extubated after the first SBT (spontaneous Breathing Trial). A patient who fails extubation is automatically classified as difficult weaning, and intensive care professionals frequently encounter patients who are difficult to wean from mechanical ventilation. Before performing a new SBT following a failed SBT, the cause of the failure should be determined and an appropriate treatment strategy developed.

Registry
clinicaltrials.gov
Start Date
March 1, 2023
End Date
July 20, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Antalya Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Sule Asri

MD

Antalya Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Invasive mechanical ventilation \> 24 hours Eligibility to weaning from mechanical ventilation

Exclusion Criteria

  • Age \< 18 years old
  • Severe skin lesions or infections that cannot perform ultrasound
  • Severe subcutaneous emphysema that cannot perform ultrasound
  • Patients with a known neuromuscular disease
  • Patients with a duration of mechanical ventilation \<24 hours,
  • Patients with severe mitral stenosis, severe mitral regurgitation, or prosthetic mitral valve

Outcomes

Primary Outcomes

Mechanical ventilation weaning success

Time Frame: 48 hours

Weaning success: stable without mechanical ventilator support during more than 48 hours

Mechanical ventilation weaning failure

Time Frame: 48 hours

Weaning failure: unstable without mechanical ventilator support within 48 hours

Secondary Outcomes

  • Mortality(ICU mortality after ultrasonography guided weaning)

Study Sites (1)

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