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| Methods | Randomized controlled trial |
| Participants | Patients scheduled for laparoscopic procedures to treat abdominal or pelvic cancer, 18 to 70 years of age, ASA status I or II, Apfel score of 3 or 4 |
| Interventions | Oral starch (control group) or 80 mg oral aprepitant (treatment group) 1 hour before induction |
| Outcomes | PONV, adverse effects |
| Notes | Study identified after the first search; data will be included in next update of the review |
