Clinical Trials Directory

Trials / Completed

CompletedNCT01443572

The Comparison of Desflurane and Sevoflurane on Postoperative Recovery and Hepatic Function of Biliary Atresia Patients During Kasai Operation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
1 Year
Healthy volunteers
Not accepted

Summary

Biliary atresia (BA) is a perinatal disease of unclear etiology, characterized by inflammation and obliteration of intrahepatic and extrahepatic bile ducts, leading to cholestasis and cirrhosis. Kasai operation remains as the first line operative treatment in BA. In the previous studies, inhalation anesthetics might induce liver damage. The choice of inhalation anesthetic that minimally affects hepatic function is important. Therefore, the purpose of this study is to compare the postoperative recovery and hepatic function between desflurane and sevoflurane, two most frequently used inhalational anesthetics in patients undergoing Kasai operation.

Conditions

Interventions

TypeNameDescription
DRUGdesflurane anesthetics40 patients are randomly allocated into two groups : desflurane group (n=20) and sevoflurane group (n=20). And anesthesia is maintained with desflurane (desflurane group) or sevoflurane (sevoflurane group).
DRUGsevoflurane anesthetics40 patients are randomly allocated into two groups : desflurane group (n=20) and sevoflurane group (n=20). And anesthesia is maintained with desflurane (desflurane group) or sevoflurane (sevoflurane group).

Timeline

Start date
2011-09-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2011-09-29
Last updated
2014-07-22

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01443572. Inclusion in this directory is not an endorsement.