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Clinical Trials in Turkey / NCT07306091
Enrolling by invitation Observational

Decanulation in Critically Ill Patients

NCT07306091 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-07-01
Last updated
2025-12-29

Condition(s) studied

Decanulation

Investigational drug(s) / intervention(s)

ultrasound guided airway examination

ultrasound guided airway examination: the position of the vocal cords (right, left, cadaveric, normal), movements with phonation and respiration, and vocal fold displacement velocity (VFDV) to control air permeability will be measured by bedside ultrasound by deflating the cuff of the tracheostomy cannula, the cannula will be removed and the same measurements will be taken again with ultrasonography, before being transferred to the otolaryngology clinic (OT) for Flexible Endoscopic Evaluation of Swallowing (FEES) exam

Study summary

Purpose of the Study: To predict potential problems (such as shortness of breath and obstruction of the airway due to vocal cord immobility) before the tracheostomy cannula is removed, the patient's vocal cords, their movement, and airflow rate will be assessed at the bedside. The patient will also be examined using routine methods to identify these problems, and the results will be compared with ultrasound scans. The study aims to determine the success and failure of ultrasound in detecting these problems. Method and Procedures: While the patient is receiving treatment in the intensive care unit, the probe of the existing ultrasound device will be placed on the patient's neck, over the cannula, and the movement of the vocal cords and airflow rate will be assessed.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criterias 1. Critically ill patients (CIPs) who are receiving treatment within the specified time period and who require a tracheostomy. 2. Critically ill patients who are suitable for decannulation (underwent spontaneous breathing trials with the use of CPAP ( CPAP level of maximum 6 cm of water and maximum 10 cm of water pressure support at least 24 hours ). 3. Critically ill patients with intact swallowing reflexes ( patients were first examined for GAG reflexes, followed by ultrasonography; changes in muscle length and contraction velocity during swallowing were measured in a sagittal section using a convex probe , 4. CIPs with GCS\>8. Exclusion Criteria: 1.Critically ill patients under 18 years of age. 2.Critically ill patients who do not require tracheostomy. 3.Critically ill patients who are spontaneously breathing and can be weaned off the ventilator for \<24 hours 4.Critically ill patients with GCS \< 8. 5.Critically ill patients with absent swallowing reflexes \-

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Uludag Universty Faculty of MedicineDepartment of Anesthesiology and Reanimation, Bursa, Turkey Bursa Turkey (Türkiye)

More Uludag University trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07306091 on ClinicalTrials.gov ↗ ← All trials in Turkey