Non-invasive carbon dioxide monitoring during robot-assisted laparoscopic surgery in steep trendeleburg position with pneumoperitoneum: transcutaneous gas monitoring vs end-tidal technique.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004680

Enrollment

Registered

2020-01-30

Start date

2020-01-23

Completion date

Unknown

Last updated

2020-02-24

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 : All subjects undergo general anesthesia under standard monitoring devices(ECG

electrocardiogram, invasive and non-invasive arterial blood pressure, SpO2

percutaneous oxygen saturation, EtCO2

end-tidal carbon dioxide, BIS, temperature etc.) and transcutaneous gas monitoring device. And subjects undergo general anesthesia in the same way as other patients who do not participate in this stud

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who undergo Robot-assisted laparoscopic surgery with steep trendelenburg position under general anesthesia American Society of Anesthesiologists physical status I–III patients Who signed informed consent

Exclusion criteria

Exclusion criteria: Aged under 19 Patients with severe cardio-pulmonary disease Body mass index(BMI) > 35kg/m2 Patients with neuromuscular disease Estimated time of operation is more than 8 hours

Design outcomes

Primary

Measure	Time frame
The PaCO2(partial pressure of carbon dioxide) by non-invasive carbon dioxide monitoring device	—

Secondary

Measure	Time frame
The PaCO2 by ABGA(arterial blood gas analysis) result;The PaCO2 by End-tidal CO2 monitoring device	—

Countries

Korea, Republic of

Contacts

Public ContactHyun Jung Lee

Ewha Womans University Seoul Hospital

Outcome results