Clinical Trial

Preemptive Analgesia in Laparoscopic Hysterectomy

Completed
View on ClinicalTrials.gov →
Summary
The aim of this study is to evaluate the effects of ibuprofen and paracetamol administered for pre-emptive analgesia to patients undergoing laparoscopic hysterectomy on pain scores during the first 24 hours postoperatively, the amount of opioids consumed postoperatively, and adverse effects such as postoperative nausea and vomiting.
Protocol Amendment History 1 change
critical Trial status changed: Not Yet Recruiting → Completed 2026-05-19
Trial Details
NCT Number NCT07401927
Lead Sponsor Giresun University
Conditions Postoperative Analgesia, Laparoscopic Hysterectomy
Enrollment 70 participants
Start Date 2026-02-02
Primary Completion 2026-04-01 (estimated)
Study Completion 2026-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-05-18