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Study identifier: NCT07002541 Synced from ClinicalTrials.gov · July 28, 2026
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PECS-II vs ESP in Nociception Level Index Guided Breast Surgery

Condition: Intraoperative Pain · Postoperative Pain  ·  Sponsor: Koç University

PhaseNA
Planned participants90
Who can joinFemale, 18 Years to 80 Years
Healthy volunteersNo

About this study

Background: Breast surgery is often associated with significant perioperative pain. While systemic opioids are commonly used, their side effects (nausea, vomiting, respiratory depression, delayed recovery) have encouraged the adoption of regional anesthesia techniques for better analgesia and reduced opioid requirements. PECS-II and Erector Spinae Plane (ESP) blocks are two effective regional techniques frequently utilized in breast surgery. However, comparative data on their impact on intraoperative opioid consumption under nociception-guided anesthesia remains limited. The Nociception Level Index (NOL) is an objective monitoring tool that integrates multiple physiological signals (e.g., heart rate variability, skin conductance, pulse amplitude) to assess nociceptive responses in real-time. When used intraoperatively, it enables more precise opioid titration, potentially optimizing analgesia while minimizing opioid exposure. Objective: To compare the efficacy of PECS-II and ESP blocks in reducing intraoperative remifentanil consumption during breast surgery under general anesthesia guided by NOL monitoring. Methods: This prospective, randomized controlled trial was conducted at Koç University Hospital following ethical approval. Ninety female patients aged 18-80 years, classified as ASA I-III and scheduled for elective mastectomy or other breast surgeries, were randomly assigned into three groups (n=30 each): Group 1 (PECS-II Block) Group 2 (ESP Block) Group 3 (Contro…

This description comes directly from the study's public registry record.

Talk to the study team

Ilayda Kalyoncu Karahan, MD  ·  +905325105014  ·  ilaydaakalyoncu@gmail.com

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Locations (1)

Koc UniversityIstanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07002541