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Clinical Trial Summary

The purpose of this study is to determine the influence of moderate FiO2 and the lung protective ventilation on postoperative pulmonary complications following hepatic resection surgery.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02198625
Study type Interventional
Source First Affiliated Hospital, Sun Yat-Sen University
Contact Fenmei Shi, M.M.
Email shifenmei2006@163.com
Status Recruiting
Phase Phase 4
Start date March 2014
Completion date June 2015

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