Effect of extraction site and local anesthesia on pain after laparoscopic appendectomy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective randomized trial compares two specimen extraction locations (periumbilical vs left lower quadrant) and the routine use of port-site local anesthesia infiltration in patients undergoing emergency laparoscopic appendectomy for acute appendicitis. Participants are randomly assigned to four groups based on extraction site and whether local anesthesia is used at trocar sites. The primary outcome is pain scores at extraction and non-extraction sites over the first 24 hours postoperatively, measured by the Numeric Rating Scale. Secondary outcomes include total analgesic use, operative time, and length of hospital stay.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients aged 18 years or older
* Diagnosed with acute appendicitis
* Scheduled for emergency laparoscopic appendectomy
* Informed consent obtained

Exclusion Criteria:

* Conversion to open surgery
* Known allergy to local anesthetics
* Cognitive impairment or inability to understand the NRS scoring system
* Pregnancy

Where it's running

• Gazi Yasargil Training and Research Hospital
  Diyarbakır, Kayapınar, Turkey (Türkiye) Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.