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Ensaio clínico

Serratus Posterior Superior Plane Block in Minimally Invasive Cardiac Surgery

NCT: NCT07420712 · COMPLETED

ID NCTNCT07420712
EstadoCOMPLETED
Data de início2026-02-20
Conclusão2026-09-01
SponsorKartal Kosuyolu High Speciality Training and Research Hospital (OTHER_GOV)
First posted
Last updated

Resumo breve

This prospective randomized controlled trial aimed to evaluate the efficacy of serratus posterior superior intercostal plane block (SPSIPB) as a component of a multimodal analgesia strategy for postoperative pain control, opioid consumption, and hemodynamic response in patients undergoing mini-thoracotomy cardiac surgery. The study was planned to include a total of 60 patients, with 30 patients in each group. Patients with ASA physical status I-III scheduled for elective mini-thoracotomy cardiac surgery (coronary artery bypass grafting, valve replacement, atrial septal defect closure, or beating-heart bypass) will be randomized to the SPSIPB group or a control group receiving standard analgesic management without any regional block. The primary outcome is the resting Numeric Rating Scale (NRS) pain score at 1 hour postoperatively. Secondary outcomes include resting and movement (passive shoulder flexion) NRS pain scores at 1, 4, 8, 16, and 24 hours, cumulative 24-hour tramadol consumption, proportion of patients requiring rescue analgesia, intraoperative remifentanil consumption, systolic blood pressure change at incision, incidence of postoperative nausea and vomiting (PONV), patient satisfaction (5-point Likert scale), time to extubation, and intensive care unit length of stay.

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