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NCT07674836
SPSIP Block Versus ESP Block for Chronic Pain After Unilateral Breast Surgery
Conditions: Postoperative Pain, Opioid Use
Sex: Female
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 90
Sponsor: Engin Çetin
Location: University of Health Sciences Kocaeli City Hospital İzmit Kocaeli
Summary
This prospective, randomized, assessor-blinded study will compare serratus posterior superior intercostal plane block and erector spinae plane block in adult female patients undergoing unilateral breast surgery. The primary outcome is chronic postoperative pain at 3 months, assessed using the Brief Pain Inventory-Short Form.
Eligibility Criteria
Inclusion Criteria:
* Female patients aged 18-65 years
* ASA physical status I-III
* Body mass index (BMI) between 18 and 35 kg/m²
* Scheduled for elective unilateral breast surgery (mastectomy with or without sentinel lymph node biopsy)
* Ability to understand and provide written informed consent
Exclusion Criteria:
* Infection at the site of block application
* Known allergy to local anesthetics
* Coagulopathy or anticoagulant therapy
* Chronic opioid use
* Pregnancy
* Inability to communicate or cooperate
* Refusal to participate
* Failed block
* Requirement of additional intraoperative analgesia outside the study protocol
* Development of serious intraoperative complications
Source: ClinicalTrials.gov (NCT07674836). StuddyBuddy aggregates publicly available trial information.