58
Participants
Start Date
December 15, 2021
Primary Completion Date
May 1, 2022
Study Completion Date
May 1, 2022
Parecoxib
Parecoxib 40mg will be administered to the experimental group if the patient has no contraindication.
Placebo
This is normal saline 2ml, which is equal to the volume of parecoxib solution. Placebo will be injected to placebo group 15 minutes before the end of the surgery.
National Taiwan University Cancer Center, Taipei
National Taiwan University Hospital
OTHER