Clinical trial Recruiting at 1 site Observational Ages 18 and up

Right-heart ultrasound to predict success of removing the breathing tube in ICU patients

Official title: Evaluation of Right Ventricular Function to Predict Weaning Success in the Intensive Care Unit: A Prospective Observational Study

Run by Kanuni Sultan Suleyman Training and Research Hospital · NCT07073976 · Data updated 2026-11-12

This study will try to see if bedside right-ventricle ultrasound measurements (like TAPSE) can predict whether adult ICU patients on mechanical ventilation will stay off the breathing tube after extubation.

More Weaning Failure of Mechanical Ventilation trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorKanuni Sultan Suleyman Training and Research Hospital
Academic / other
Locations1 site (Istanbul, Istanbul)
StatusRecruiting
StartedJuly 31, 2025
Main results expectedJuly 15, 2026
Study endsJuly 16, 2026
Registry record updatedSeptember 9, 2025
Trial IDNCT07073976 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult ICU patients receiving invasive mechanical ventilation who are hemodynamically stable, meet standard clinical weaning criteria, can undergo transthoracic echocardiography within two hours before extubation, and provide informed consent are ideal candidates.

Probably not a fit

Patients with inadequate acoustic windows, severe tricuspid or congenital valve disease, on extracorporeal life support, with acute pulmonary embolism or cor pulmonale, those requiring urgent/unplanned extubation, or pregnant patients are unlikely to benefit from the protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, observational single-center study in adult ICU patients planned for weaning from mechanical ventilation. Bedside transthoracic echocardiography will be performed within two hours after patients meet clinical weaning criteria to measure TAPSE, tricuspid S', RV-FAC, right atrial area, and pulmonary valve acceleration time. Patients will be followed for 24 hours after extubation to record reintubation, need for noninvasive ventilation or high-flow oxygen, and other respiratory/physiologic data. Demographic and clinical variables (APACHE II, SOFA, ventilation settings, duration of ventilation) will be collected to relate cardiac measurements to weaning outcomes.

Why it matters

Potential benefit: If successful, the approach could help clinicians identify patients at higher risk of failed extubation and tailor weaning decisions to reduce reintubation and complications.

How similar studies have gone: Prior observational studies have linked right ventricular dysfunction and measures like TAPSE to weaning failure, but results are mixed and prospective single-center validation remains limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Receiving invasive mechanical ventilation in the ICU
* Planned extubation (weaning) according to standard clinical criteria
* Hemodynamically stable at the time of transthoracic echocardiography (TTE)
* Ability to undergo echocardiographic assessment within 2 hours prior to extubation
* Informed consent obtained from patient or legal representative

Exclusion Criteria:

* Known severe tricuspid valve disease or congenital heart disease
* Moderate to severe pericardial effusion or cardiac tamponade
* Inadequate acoustic window for transthoracic echocardiography
* Patients requiring urgent or unplanned extubation
* Use of extracorporeal life support (e.g., ECMO) at the time of assessment
* Known pulmonary embolism or acute cor pulmonale
* Pregnancy

Where it's running

  • Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
    Istanbul, Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.