CompletedNot Applicable

Erector Spinae Plane Block Versus Thoracic Paravertebral Block in Laparoscopic Cholecystectomy

Turkey (Türkiye)120 participantsStarted 2025-09-01

Plain-language summary

The study is planned as a single-center prospective randomized study and includes patients undergoing laparoscopic cholecystectomy. The aim of this study is to compare postoperative analgesic efficacy of erector spinae plane block and thoracic paravertebral block. Primary outcome is 24-hour postoperative opioid consumption.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Elective cholecystectomy * Age \>18years * American Society of Anesthesiologists classification I-III Exclusion Criteria: * Presence of contraindications for using regional anesthesia ( not having patient approval, bleeding diathesis or use of anticoagulants, infection at the injection site, and allergy to local anesthetics) * Chronic analgesic use * Open cholecystectomy or conversion to open cholecystectomy

What they're measuring

Tramadol consumption

Timeframe: postoperative 24 hours

Trial details

NCT IDNCT07149584

SponsorIstanbul University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-02-23

View on ClinicalTrials.gov More Pain, Acute Postoperative trials