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Preemptive Analgesia in Laparoscopic Hysterectomy

NCT07401927 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2026-05-18

No results posted yet for this study

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.

Conditions

  • Postoperative Analgesia
  • Laparoscopic Hysterectomy

Interventions

DRUG

Ibuprofen

Administered as part of standard institutional anesthesia practice.

DRUG

Parasetamol

Administered as part of standard institutional anesthesia practice.

Sponsors & Collaborators

  • Giresun University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-02
Primary Completion
2026-04-01
Completion
2026-05-01

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07401927 on ClinicalTrials.gov