Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06688019

A Comparison of High-flow Nasal Oxygen and Conventional Nasal Cannula in Monitored Anesthesia Care for Endoscopic Submucosal Dissection

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

Sedation for endoscopic submucosal dissection places patients at risk of desaturation, and high-flow nasal oxygen may reduce the risk. The aim of this study is to evaluate the role of high-flow nasal oxygen during endoscopic submucosal dissection. We will compare the incidence of hypoxemia (defined as SpO2 lower than 90%) of conventional nasal oxygen cannula group and that of high-flow humidified oxygen-delivery system group during the procedure.

Conditions

Interventions

TypeNameDescription
DEVICEconventional oxygenation (nasal cannula)conventional oxygenation arm will receive oxygen at 2 L/min via nasal cannula, while Optiflow THRIVE arm will receive oxygen at 50 L/min via Optiflow THRIVE during the procedure.
DEVICEhigh-flow humidified oxygen-delivery system (OptiFlow THRIVE)conventional oxygenation arm will receive oxygen at 2 L/min via nasal cannula, while Optiflow THRIVE arm will receive oxygen at 50 L/min via Optiflow THRIVE during the procedure.

Timeline

Start date
2024-11-01
Primary completion
2025-10-18
Completion
2025-10-18
First posted
2024-11-14
Last updated
2024-11-14

Source: ClinicalTrials.gov record NCT06688019. Inclusion in this directory is not an endorsement.