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

• Register: ClinicalTrials.gov
• Last refreshed on: 19 February 2015
• Main ID: NCT01443572
• Date of registration: 16/09/2011
• Prospective Registration: No
• Primary sponsor: Yonsei University
• Public title: The Comparison of Desflurane and Sevoflurane on Postoperative Recovery and Hepatic Function of Biliary Atresia Patients During Kasai Operation
• Date of first enrolment: September 2011
• Target sample size: 40
• Recruitment status: Completed
• URL: http://clinicaltrials.gov/show/NCT01443572
• Study type: Interventional
• Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
• Phase: N/A

Countries of recruitment

Korea, Republic of

Key inclusion & exclusion criteria

Inclusion Criteria:

- patients with biliary atresia undergoing Kasai operation

Exclusion Criteria:

- patients with congenital anomalies at major organs



Age minimum: N/A
Age maximum: 1 Year
Gender: Both

Health Condition(s) or Problem(s) studied

Biliary Atresia

Kasai Operation

Intervention(s)

Drug: sevoflurane anesthetics

Drug: desflurane anesthetics

Primary Outcome(s)

Change in hepatic function [Time Frame: after operation, and on the 1st, 2nd, 3rd, 5th, 7th and 15th postoperative days]

Change in postoperative recovery [Time Frame: after operation, and on the 1st, 2nd, 3rd, 5th, 7th and 15th postoperative days.]

Secondary ID(s)

4-2011-0436

Source(s) of Monetary Support

Please refer to primary and secondary sponsors