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Clinical Trial Summary

In this study, the investigators measure a pupil size every 5 minutes during the operation in patients undergoing laparoscopic cholecystectomy under general anesthesia. The investigators would compare the postoperative pain intensity between the group adjusted the anesthetic drug concentration based on the changes of the pupil (Pupil group) and the group based on the changes of a surgical pleth index (SPI group).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03794271
Study type Interventional
Source Daegu Catholic University Medical Center
Contact
Status Completed
Phase N/A
Start date January 3, 2019
Completion date May 10, 2019

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