Anesthesiology Department, Faculty of Medicine, Prince of Songkla University
Hat Yai, Changwat Songkhla, 90110, Thailand
NCT Number: NCT01543945
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.
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Notify Me18 year–45 year
Female
Interventional
Phase 2
Hat Yai, Changwat Songkhla, 90110, Thailand
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
4 mg iv before induction for high and extremely high risk
Other names: Multimodal antiemetic group :, high risk : dexamethasone 4 mg + ondansetron 4 mg, Extremely high risk : dexamethasone 4 mg +, ondansetron 4 mg +, dimenhydrinate 1 mg
4 mg iv before ended surgery 30 min
1 mg/kg iv before ended surgery 30 min
Time frame: four year
Prince of Songkla University
Other
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