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Clinical Trial Summary

To compare postoperative pain, opioid consumption and chronic pain in patients undergoing to hernia repair surgery after receiving nitrous oxide or oxygen during the general anesthesia.


Clinical Trial Description

The study is prospective and double blind. In the clinic, patients undergoing inguinal hernia surgery that meet the criteria for inclusion into the study and agreed to participate in the study will be randomized into two groups. In the first group of patients will receive Nitrous Oxide and In the second group of patients will receive oxygen during the general anesthesia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01622322
Study type Interventional
Source The Cleveland Clinic
Contact
Status Withdrawn
Phase N/A
Start date May 2012
Completion date December 2023

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