Actively Recruiting
POCUS Assessment for Differentiating Tracheal Versus Oesophageal Intubation During Surgery
Led by Clinica Universidad de Navarra, Universidad de Navarra · Updated on 2026-04-14
200
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the use of Point-of-Care Ultrasound (PoCUS) to distinguish between tracheal and oesophageal intubation during airway management. This observational study focuses on improving the accuracy of confirming correct endotracheal tube placement, which is crucial to avoid serious complications. The study builds on existing methods like capnography and aims to provide a simple, quick ultrasound approach that complements current practices. The study involves using an ultrasound transducer placed on the front of the neck to locate the oesophagus and observe the tube's passage into the trachea in real time during orotracheal intubation. This ultrasound technique is compared with capnography or lung sliding to verify correct tube placement. The procedure is applied to patients undergoing scheduled or emergency surgeries requiring intubation. Participants will be monitored during the intubation process, with ultrasound used to confirm tube placement within minutes. Researchers will assess the accuracy of ultrasound detection of oesophageal intubation and also evaluate the learning curve for using PoCUS in this context. The study is expected to conclude by August 2026, and participants include adults aged 18 to 90 years undergoing relevant surgical procedures.
CONDITIONS
Brief Title
POCUS ASSESSMENT FOR TRACHEAL VS OESOPHAGEAL INTUBATION
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 and 90 years
- Male or female patients classified as ASA I-III
- Undergoing scheduled or emergency surgery requiring orotracheal intubation
- Signed informed consent form authorizing inclusion in the study
You will not qualify if you...
- Presence of cervical tumors, goitre, or history of cervical radiotherapy
- Facial or cervical fractures causing anatomical alterations
- Inability to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 5 minutes during surgery
Participants undergo ultrasound assessment to differentiate tracheal versus oesophageal intubation during surgery.
1 visit (in-person during surgery)
Trial Site Locations
Total: 1 location
1
Clinica Universidad de Navarra
Madrid, Madrid, Spain, 28027
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1