Clinical Trial

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

Recruiting Phase 3
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Record status
This record was last updated March 3, 2026 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.
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.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-11-18; most recent amendment 2026-02-27.
Status change: Not Yet Recruiting → Recruiting 2026-02-27
Trial Details
NCT Number NCT07248280
Lead Sponsor Centre hospitalier de l'Université de Montréal (CHUM)
Conditions Nausea and Vomiting, Postoperative, Prevention
Enrollment 260 participants
Start Date 2026-02-27
Primary Completion 2026-07-01 (estimated)
Study Completion 2027-01-01 (estimated)
Updated on ClinicalTrials.gov 2026-03-03