The purpose of this study is to compare the incidence of Postoperative nausea and vomiting between the intervention group who received multimodal antiemetic management and the control group who did not get this protocol.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
340
4 mg iv before induction for high and extremely high risk
4 mg iv before ended surgery 30 min
1 mg/kg iv before ended surgery 30 min
Anesthesiology Department, Faculty of Medicine, Prince of Songkla University
Hat Yai, Changwat Songkhla, Thailand
Incidence of PONV in ambulatory gynecologic laparoscopy
Time frame: four year
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