Postoperative Nausea and Vomiting in Laparoscopic Abdominal Surgery

Sex: All

Ages: 18 Years – 90 Years

Healthy volunteers: 1

Phase: PHASE4

Enrollment: 60

Sponsor: Baskent University

Summary

The goal of this clinical trial is to compare frequency with postoperative nausea and vomiting in ASA( American Society of Anesthesiologists) I, II patients undergoing laparoscopic surgery.The main question[s] it aims to answer are:Primary Outcome is the incidence of nausea and vomiting between 0-6 and 6-24 hours postoperatively and the need for additional antiemeticsSecondary outcome is detection of additional analgesic needs and complications between 0-6 and 6-24 hours postoperatively.Participants will receive aprepitant or granisetron for prevention of postoperative nausea and vomiting.

Eligibility Criteria

Inclusion Criteria:ASA I, II patients patients undergoing laparoscopic surgeryExclusion Criteria:ASA III and above patients who refused to participate in the study

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05632224). StuddyBuddy aggregates publicly available trial information.