About this trial
This prospective, randomized clinical study aims to compare the analgesic efficacy of the interpectoral-pectoserratus plane block and the serratus posterior superior intercostal plane block for postoperative pain management in patients undergoing breast cancer surgery. Both techniques are ultrasound-guided regional anesthesia methods targeting different interfascial planes of the thoracic wall. The study will evaluate postoperative pain scores, opioid consumption, Quality of recovery and potential complications. The findings are expected to contribute to optimizing regional anesthesia strategies for enhanced recovery and improved analgesia following breast cancer surgery.
Eligibility criteria
Qualifiers
18-65 years of age
ASA I-II-III risk groups
Patients with informed consent
Patients undergoing breast cancer surgery
Disqualifiers
ASA ≥ IV
History of allergy to local anesthetics
Known coagulation disorders
Infection near the insertion site
Trial design
Treatments tested in this trial
- Interpectoral-Pectoserratus Plane Block
- Serratus Posterior Superior Intercostal Plane Block