Skip to main content
Clinical Trials/ACTRN12616000672459
ACTRN12616000672459
Completed
Phase 4

The effect of intravenous pre-emptive versus postoperative paracetamol on postoperative nausea and vomiting in children undergoing strabismus surgery: A prospective randomised study

Mehmet AKSOY0 sites90 target enrollmentStarted: May 23, 2016Last updated:

Overview

Phase
Phase 4
Status
Completed
Sponsor
Mehmet AKSOY
Enrollment
90

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Prevention
Masking
Blinded (masking used)

Eligibility Criteria

Ages
2 Years to 14 Years (—)
Sex
All

Inclusion Criteria

  • Ninety\-six patients, between the ages of 2 and 14 years,ASA (the classification of the American Society of Anesthesiologists) physical status I\-II who underwent elective strabismus surgery under general anaesthesia were included

Exclusion Criteria

  • Patients with a history of allergy to any of the study medications (general anesthetic agents or paracetamol), with a history of previous PONV or motion sickness, hepatic or renal disease, use of antiemetic, antihistaminic, analgesic or corticosteroid 24 hours prior to surgery and were excluded from the study.

Investigators

Sponsor
Mehmet AKSOY

Similar Trials