Clinical Trial

Parasternal and Adductor Canal Blocks in CABG

Not Yet Recruiting
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Summary
This randomized controlled trial evaluates the effectiveness of different postoperative analgesic strategies in patients undergoing coronary artery bypass graft (CABG) surgery. Patients were allocated into three groups receiving either conventional analgesia alone, parasternal block in addition to conventional analgesia, or combined parasternal and adductor canal blocks with conventional analgesia. The study aims to compare postoperative pain scores, opioid consumption, and recovery outcomes among the groups in order to determine whether the addition of regional anesthesia techniques, particularly the combined block approach, provides superior analgesia and enhances postoperative recovery following CABG surgery.
Trial Details
NCT Number NCT07599748
Lead Sponsor Zonguldak Bulent Ecevit University
Conditions Postoperative Pain, Regional Anaesthsia, Pain Management
Enrollment 120 participants
Start Date 2026-06-15
Primary Completion 2027-04-01 (estimated)
Study Completion 2027-07-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-20