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Clinical Trials in Turkey / NCT07824908
Recruiting Not applicable

Effect Of Specimen Extraction Site And Local Anesthesia On Postoperative Pain In Laparoscopic Appendectomy

NCT07824908 · tracked via the Priya Life Science Turkey tracker
Sponsor
YUNUS YÜKSEL
Phase
Not applicable
Started
2026-04-24
Last updated
2026-09-17

Condition(s) studied

Appendectomy, LaparoscopicAppendicitis AcutePain Management

Investigational drug(s) / intervention(s)

Port-site local anesthesia infiltrationPort-Site Saline Infiltration (Placebo)

Port-site local anesthesia infiltration: Infiltration of local anesthetic solution (bupivacaine) into the skin, subcutaneous tissue, and fascial layers of all trocar sites prior to closure

Port-Site Saline Infiltration (Placebo): Prior to wound closure, a total of 10 cc of %0.9 normal saline solution is infiltrated into the skin, subcutaneous tissues, and fascial layers of all trocar sites as a placebo control

Study summary

The aim of this prospective, randomized study is to evaluate the effects of two different specimen extraction sites (periumbilical versus left lower quadrant) and the routine application of port-site local anesthesia infiltration on postoperative pain and complications in patients undergoing laparoscopic appendectomy for acute appendicitis."

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gazi Yasargil Training and Research Hospital Diyarbakır Kayapınar Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07824908 on ClinicalTrials.gov ↗ ← All trials in Turkey