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Clinical Trials in Turkey / NCT07611903
Recruiting Not applicable

HFNC Versus Microstream Advance Nasal Cannula for Oxygenation During ERCP

NCT07611903 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-07-14
Last updated
2026-07-15

Condition(s) studied

Endoscopic Retrograde CholangiopancreatographyHypoxemia

Investigational drug(s) / intervention(s)

High-flow nasal canulaMicrostream advance nasal cannula

High-flow nasal canula: Heated and humidified high-flow oxygen therapy delivered through a nasal cannula during ERCP under sedation

Microstream advance nasal cannula: Oxygen support delivered through the Microstream Advance nasal cannula during ERCP under sedation.

Study summary

Endoscopic retrograde cholangiopancreatography (ERCP) procedures are commonly performed under deep sedation and are associated with a risk of hypoxemia, particularly in prone or semi-prone positions. High-flow nasal cannula (HFNC) therapy may improve oxygenation by delivering heated and humidified oxygen at high flow rates, while the Microstream Advance nasal cannula provides simultaneous nasal oxygen delivery and oral oxygen insufflation.

This prospective randomized study aims to compare the effectiveness of HFNC and Microstream Advance nasal cannula in maintaining oxygenation during ERCP procedures. Patients undergoing ERCP will be randomized into two groups receiving either HFNC or Microstream Advance nasal cannula oxygen support during sedation.

The primary outcomes are the incidence of desaturation and oxygen reserve index (ORi) measurements during the procedure. Secondary outcomes include time to achieve target ORi levels, respiratory complications, and procedure-related adverse events.

Eligibility

Sex
ALL
Min age
18 Years
Max age
84 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 to 84 years * ASA physical status I-III * Patients scheduled to undergo ERCP * Patients who provide written informed consent Exclusion Criteria: * Recent history of upper respiratory tract infection * History of lung cancer * Chronic obstructive pulmonary disease * Asthma * Body mass index greater than 35 kg/m² * Refusal to participate in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kocaeli University Faculty of Medicine Hospital Kocaeli Umuttepe Recruiting

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Other trials for the same condition

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 NCT07611903 on ClinicalTrials.gov ↗ ← All trials in Turkey