66
Participants
Start Date
April 20, 2018
Primary Completion Date
August 5, 2018
Study Completion Date
October 31, 2018
Experimental group
In subjects allocated to the abdominal binder group, the abdomen binder with a standard height of 22 cm (Sejung Korea, Seoul, Republic of Korea) was applied before leaving the operating room. The binder was placed on the abdomen across the laparoscopic incision, with the upper border not higher than the lower margin of the rib cage, ensuring minimal restriction of lateral costal expansion and diaphragmatic excursion. Subjects were carefully instructed to use the abdominal binder during at least the first 2 consecutive days and night, and to reposition the abdominal binder correctly when needed.
Control group
In subjects allocated in the control group, subjects were not given any opportunity to ware an abdominal binder.
Kangbuk Samsung Hospital, Seoul
Kangbuk Samsung Hospital
OTHER