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Critical Care Ultrasound Guided Weaning

Critical Care Ultrasound Guided Weaning

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05763134
Enrollment
27
Registered
2023-03-10
Start date
2023-03-01
Completion date
2023-07-20
Last updated
2023-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weaning Failure

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.

Interventions

None listed

Sponsors

Antalya Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Mechanical ventilation weaning success48 hoursWeaning success: stable without mechanical ventilator support during more than 48 hours
Mechanical ventilation weaning failure48 hoursWeaning failure: unstable without mechanical ventilator support within 48 hours

Secondary

MeasureTime frameDescription
MortalityICU mortality after ultrasonography guided weaningIncidence of ICU mortality

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026