IPP-PSP Block vs. SPSIPB in Breast Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorZonguldak Bulent Ecevit University

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

Treatment groups

70 Participants
are divided into 2 treatment groups