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Clinical Trial Summary

To meet the needs of both operators and patients, moderate and deep sedation has been widely used in digestive endoscopy, which is invasive and painful. With its pleasant effects, sedation has complications nevertheless. And respiratory depression is the most common one, which makes respiratory monitoring significant. SpO2 and respiratory motion are regularly monitored without satisfying timeliness or sensitivity. Capnography with current device is only able to detect either oral or nasal breathing. The present study was designed to test the effect of the investigator's modified End-Tidal Carbon Dioxide (ETCO2) monitoring device for sedation during endoscopic ultrasonography-guided fine needle aspiration.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT04549623
Study type Interventional
Source Changhai Hospital
Contact Jia-feng Wang, MD
Phone +862131161869
Status Recruiting
Phase N/A
Start date September 27, 2020
Completion date February 2022

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