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Study identifier: NCT06637280 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

High - Flow Nasal Cannula Versus Conventional Nasal Cannula During Endobronchial Ultrasound Procedure

Condition: Hypoxemia During EBUS Bronchoscopy  ·  Sponsor: The University Clinic of Pulmonary and Allergic Diseases Golnik

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

EBUS bronchoscopy is performed in most centers under local anesthesia and moderate sedation. Both the bronchoscopy itself and the sedation can lead to decreased ventilation and a drop in oxygen saturation in the body. Typically, oxygen is administered during the procedure via a nasal cannula at a flow rate of 6l/min. The aim of the study is to compare a new method - a nasal cannula with high flow - to the standard cannula. The primary objective is to demonstrate that the new method is more effective at preventing desaturation during the procedure. Patients will be randomized into two groups before bronchoscopy and monitored. The bronchoscopy will be performed in the same way for both groups. The only difference between the groups will be in the method of oxygen administration during EBUS bronchoscopy.

This description comes directly from the study's public registry record.

Talk to the study team

Ales Rozman, MD, PhD  ·  +38641313811  ·  ales.rozman@klinika-golnik.si

Sonja Badovinac, MD, PhD  ·  +385916302152  ·  sonjabadovinac1@gmail.com

Always discuss trial participation with your own doctor first.

Locations (4)

University Hospital Centre Zagreb - JordanovacZagreb, City of Zagreb, CroatiaRecruiting
National and Kapodistrian University of AthensAthens, Athens, GreeceRecruiting
Clinica Universitaria de Pneumologia, Hospital de Santa MariaLisbon, Lisbon District, PortugalRecruiting
University Clinic GolnikGolnik, Golnik, SloveniaRecruiting

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Source record: clinicaltrials.gov/study/NCT06637280