Effect of Abdominal Binder aftEr Laparoscopic Treatment on Postoperative Recovery

NACompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

April 20, 2018

Primary Completion Date

August 5, 2018

Study Completion Date

October 31, 2018

Conditions
Laparoscopy
Interventions
DEVICE

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.

DEVICE

Control group

In subjects allocated in the control group, subjects were not given any opportunity to ware an abdominal binder.

Trial Locations (1)

03181

Kangbuk Samsung Hospital, Seoul

All Listed Sponsors
lead

Kangbuk Samsung Hospital

OTHER

NCT03485859 - Effect of Abdominal Binder aftEr Laparoscopic Treatment on Postoperative Recovery | Biotech Hunter | Biotech Hunter