53
Participants
Start Date
February 1, 2018
Primary Completion Date
December 1, 2019
Study Completion Date
February 1, 2020
1000 mL 0.9% sterile saline
Within 12 h of surgery, the experimental group received 1000 mL 0.9% sterile saline intravenously.
250 mL 0.9% sterile saline
Within 12 h of surgery, the control group received 250 mL 0.9% sterile saline intravenously.
Tri-Service General Hospital, National Defense Medical Center, Taipei
Tri-Service General Hospital
OTHER