Is EtCO2 monitoring beneficial in predicting hypoxemia during ESD procedures?

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0003817

Enrollment

506

Registered

2019-04-18

Start date

2018-09-17

Completion date

Unknown

Last updated

2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : INTERVENTION group : Conventional peripheral O2 saturation monitoring + Exhaled CO2 monitoring CONTROL group : Conventional peripheral O2 saturation monitoring ONLY

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Ages 18 ~ 70 ASA (American Society of Anesthesiologists) class 1-3 Ability to give written informed consent

Exclusion criteria

Exclusion criteria: Allergy to midazolam or propofol ASA class 4 or 5 Unable to give informed consent Pregnant women Pre-existing hypotension (systolic BP < 90mmHg) Pre-existing bradycardia (HR < 50 bpm), hypoxemia (SpO2 < 90%) Acute respiratory illness Recent otorhinolaryngologic surgery

Design outcomes

Primary

Measure	Time frame
Occurence of alteration in EtCO2 and hypoxia	—

Secondary

Measure	Time frame
Total procedure time and total dose of sedatives	—

Countries

Korea, Republic of

Contacts

Public ContactSang Hoon Kim

Korea University Anam Hospital

spring0107@naver.com+82-2-920-6555

Outcome results