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Starting soon Not applicable

The Effect of Nerve Blocks on Analgesia in Breast Cancer Surgery

NCT07601490 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-15
Last updated
2026-05-27

Condition(s) studied

Breast Cancer Surgery Pain

Investigational drug(s) / intervention(s)

Serratus Posterior Superior Intercostal Plane BlockSerratus anterior plane block (SAP)

Serratus Posterior Superior Intercostal Plane Block: Ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block performed preoperatively for postoperative analgesia in modified radical mastectomy surgery.

Serratus anterior plane block (SAP): Ultrasound-guided Serratus Anterior Plane (SAP) block performed preoperatively for postoperative analgesia in modified radical mastectomy surgery.

Study summary

Postoperative pain following modified radical mastectomy remains a significant clinical concern and may adversely affect patient recovery, opioid consumption, and overall patient satisfaction. Ultrasound-guided regional anesthesia techniques have gained increasing importance as part of multimodal analgesia strategies in breast surgery. The serratus anterior plane (SAP) block is a commonly used interfascial plane block for postoperative analgesia in thoracic and breast procedures. Recently, the serratus posterior superior intercostal plane (SPSIP) block has emerged as a novel regional anesthesia technique with potentially wider thoracic dermatomal spread and effective analgesic properties.

This prospective randomized controlled study aims to compare the postoperative analgesic efficacy of the SPSIP block and SAP block in patients undergoing modified radical mastectomy under general anesthesia. Patients will be randomly allocated into two groups to receive either ultrasound-guided SPSIP block or SAP block preoperatively. Primary outcomes will include postoperative pain scores and opioid consumption within the first 24 hours after surgery. Secondary outcomes will include time to first analgesic request, rescue analgesic requirements, intraoperative hemodynamic parameters, postoperative nausea and vomiting, block-related complications, and patient satisfaction.

The study is designed to evaluate whether SPSIP block provides superior postoperative analgesia compared with SAP block in modified radical mastectomy surgery.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Female patients aged between 18 and 65 years * American Society of Anesthesiologists (ASA) physical status I-III * Body Mass Index (BMI) \<35 kg/m² * Normal International Normalized Ratio (INR) value and platelet count * Normal liver and renal function tests * Patients scheduled for elective modified radical mastectomy surgery Exclusion Criteria: * Bleeding diathesis * Allergy to local anesthetic agents * Suspected infection or inflammation at the planned block site * ASA physical status IV or higher * Long-term medication use due to chronic pain * Advanced hepatic or renal failure * Presence of severe pulmonary disease * Use of any opioid medication within 24 hours before surgery * Cognitive impairment * Patients undergoing revision surgery

Primary outcome measure(s)

  • Postoperative pain intensity assessed by Visual Analog Scale (VAS) — At postoperative 1, 2, 4, 8, 12, and 24 hours after surgery
    Postoperative pain intensity will be evaluated using the Visual Analog Scale (VAS), a 10-point scale ranging from 0 to 10, where 0 indicates "no pain" and 10 indicates "the worst imaginable pain." VAS scores at rest and during movement will be recorded and compared between patients receiving ultrasound-guided superior posterior serratus intercostal plane (SPSIP) block and serratus anterior plane (SAP) block following modified radical mastectomy surgery. Higher VAS scores indicate greater pain severity and poorer analgesic efficacy.

Trial sites (1)

FacilityCityRegionStatus
Health Sciences University 2. Sultan Abdülhamid Han Training and Research Hospital Istanbul Uskudar

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07601490 on ClinicalTrials.gov ↗ ← All trials in Turkey