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Clinical Trial Summary

The aim of the study was to evaluate the preoxygenation time by observing patients undergoing preoxygenation with CPAP (Continuous Positive Airway Pressure) and Mask Ventilation in the clinic.


Clinical Trial Description

Criteria for inclusion in the study:

Planned elective bariatric surgery under general anesthesia ASA 1-2 class Between 20-50 years 50 patients

1. Group: Patients undergoing CPAP (Continuous Positive Airway Pressure) during preoxygenation will be included.

2. Group: Patients undergoing preoxygenation without CPAP will be included

In both groups, the time from the anesthesia device to the endtidal O2 90% and the endtidal CO2 value in this order will be recorded.

Heart rate, blood pressure, endtidal O2 and CO2 values will be recorded during preoxygenation and after intubation. ;


Study Design


Related Conditions & MeSH terms

  • Time to Reach 90% Endtidal Oxygen During Preoxygenation

NCT number NCT03807375
Study type Interventional
Source Ankara Diskapi Training and Research Hospital
Contact
Status Completed
Phase N/A
Start date March 1, 2018
Completion date June 1, 2019