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NCT07246720

IPP-PSP Block vs. SPSIPB in Breast Surgery

Not Yet Recruiting · Not Applicable · Zonguldak Bulent Ecevit University · registry updated 2025-11-24

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

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.

Inclusion

  • years of age
  • ASA I-II-III risk groups
  • Patients with informed consent
  • Patients undergoing breast cancer surgery

Exclusion

  • Exclusion Criteria: • Ages \<18 and \>65
  • History of allergy to local anesthetics
  • Known coagulation disorders
  • Infection near the insertion site
  • Chronic analgesic use
  • Patients with diabetes mellitus and those receiving neoadjuvant chemotherapy (due to potential impairment of pain sensation)

Open NCT07246720 on ClinicalTrials.govAll conditions