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Clinical Trial Summary

The endotracheal intracuff pressure is to be maintained at a low level to prevent trachea and nerve damages, and yet be high enough to secure air sealing. The objective of the study is to compare minimal occlusive volume technique (MOVT) and expired volume/inspired volume ratio (VE/VI ratio) from a spirometer method of endotracheal tube (ETT) cuff inflation with respect to the cuff pressure required to seal the airway during a laparoscopic surgery under general anesthesia. A study design is a randomized crossover trial in 35 patients. The primary outcome is the intracuff pressure of an endotracheal tube. The study consists of two cuff sealing methods separated by a period of 10 minutes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03385044
Study type Interventional
Source DongGuk University
Contact
Status Completed
Phase N/A
Start date March 12, 2018
Completion date October 29, 2018

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