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NOT YET RECRUITING
NCT06543966
PHASE3

Efficacy and Safety Study of Aprepitant Injection for Prevention of Post-operative Nausea and Vomiting

Sponsor: CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.

View on ClinicalTrials.gov

Summary

A randomized, double-blind, placebo-controlled, multi-center phase III study to compare the efficacy and safety of aprepitant injection and placebo in the prevention of post-operative nausea and vomiting (PONV).,

Official title: A Randomized, Double-blind, Placebo-controlled, Multi-center Phase III Study to Evaluate the Efficacy and Safety of Aprepitant Injection in the Prevention of Post-operative Nausea and Vomiting

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

486

Start Date

2024-10-28

Completion Date

2026-03-28

Last Updated

2024-08-09

Healthy Volunteers

No

Interventions

DRUG

Aprepitant Injection

Before anesthesia induction, 4.4ml(32mg) was given by a single intravenous injection, which was completed within 30 seconds

DRUG

Aprepitant Injection Placebo

Before anesthesia induction, 4.4ml(0mg) was given by a single intravenous injection, which was completed within 30 seconds