NCT07248280

Adding Aprepitant to a Multimodal Strategy for the Prevention of Postoperative Nausea and Vomiting in High-risk Outpatient Surgical Patients

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Registry fields

Overall status
COMPLETED
Conditions
Nausea and Vomiting, Postoperative, Prevention
Study type
INTERVENTIONAL
Phase
PHASE3
Primary purpose
PREVENTION
Intervention type
DRUG
Interventions
Aprepitant 40mg, Placebo
Lead sponsor
Centre hospitalier de l'Université de Montréal (CHUM) (OTHER)

Cached at: 2026-08-28 23:27:21

View on ClinicalTrials.gov

Brief summary

Postoperative nausea and vomiting (PONV) are a frequent and debilitating complications after surgery, affecting up to 80% of patients at high risk in the absence of prophylaxis.

Despite the rigorous application of the recommendations from the American Society of Anesthesiologists (ASA) at CHUM, a recent local study reveals a prevalence of 25% PONV at home after outpatient surgery. However, the therapeutic options at home remain limited.

This study aims to evaluate if the addition of 40 mg aprepitant to a multimodal strategy for preventing PONV improves clinical outcomes in high-risk patients undergoing outpatient surgery.

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