Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
FEMALE
NCT07368413

Comparison of the Analgesic Efficacy of Erector Spinae Plane Block in Breast-Conserving Surgery Versus Serratus Anterior Block Combined With Additional Pecto-Intercostal II Block

Led by Kayseri City Hospital · Updated on 2026-04-21

70

Participants Needed

1

Research Sites

16 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective randomized study will compare the effects of Erector Spinae Plane Block (ESPB) and Serratus Anterior Plane Block combined with Pectoral Nerve Block Type II (SAPB + PECS II) on intraoperative analgesia and postoperative opioid consumption in patients undergoing breast cancer surgery. Seventy patients (ASA I-III, aged 18-75 years) will be randomized into two groups using the sealed envelope method. Ultrasound-guided blocks will be performed preoperatively by the same anesthesiologist, with Group 1 receiving ESPB and Group 2 receiving a combined SAPB + PECS II technique performed through a single skin puncture (single needle entry site) with sequential injections into the two target fascial planes. All patients will undergo surgery under general anesthesia and receive postoperative analgesia via morphine patient-controlled analgesia. Pain scores and total opioid consumption will be statistically analyzed, with p \< 0.05 considered significant.

CONDITIONS

Official Title

Comparison of the Analgesic Efficacy of Erector Spinae Plane Block in Breast-Conserving Surgery Versus Serratus Anterior Block Combined With Additional Pecto-Intercostal II Block

Who Can Participate

Age: 18Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 75 years
  • ASA physical status I-III
  • No history of bleeding or coagulation disorders
  • No neuropathy
  • Preoperative breast region pain score less than 4 on the Numerical Rating Scale
Not Eligible

You will not qualify if you...

  • Presence of systemic or regional infection
  • Known allergy to local anesthetics
  • Unwillingness to participate in the study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Kasyeri City Hospital

Kayseri, Kocasinan, Turkey (Türkiye), 38080

Actively Recruiting

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Research Team

E

Erdoğan Rahmi Çinçin, Resident Doctor

CONTACT

Ç

Çiğdem Ünal Kantekin, Associate Professor of Medicin

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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