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Completed

NCT Number: NCT06177665

Comparison of Erector Spina Plan Block and Rhomboid Intercostal Block in Breast Surgery

In this study, the investigators compared ultrasound-guided erector spinae plane (ESP) block and rhomboid intercostal block (RIB) on postoperative analgesic effect in unilateral breast surgery.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Kocaeli University

Kocaeli, Turkey (Türkiye)

About this study

After being informed about the study and potential risks, written consent was obtained from all patients.Patients who meet eligibility requirements will be randomized in a 1:1 ratio to erector spinae plane block and rhomboid intercostal block.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who will undergo unilateral breast-conserving surgery (BCS) or modified radical mastectomy (MRM) with or without axillary lymph node dissection
  • Patients undergoing elective surgery
  • ASA (American Society of Anesthesiologists) physical status classification I-III

Exclusion criteria

  • Use of anticoagulants
  • Allergy to the medications to be used
  • Patients who use analgesic drugs due to a history of chronic pain
  • ASA (American Society of Anesthesiologists) physical status classification IV-V
  • Patients with psychiatric disorders
  • Presence of infection in the area where the block will be applied
  • Presence of deformity in the patient's spinal, paraspinal and area where the block will be applied
  • The patient does not accept the block application or cannot cooperate with the patient

Treatment and study plan

Erector spinae plane block

Other

Ultrasound(US)-guided erector spinae plan block(ESP) with 20 ml 0,25% bupivacaine at T4 vertebra level will performe preoperatively to all patients in the ESP group.

Rhomboid intercostal block

Other

Ultrasound(US)-guided rhomboid intercostal block(RIB) with 20 ml 0,25% bupivacaine at T5-T6 vertebra level will performe preoperatively to all patients in the RIB group.

Primary outcomes

  1. Morphin Consumption

    Time frame: during postoperative 24 hours

    Patients in both groups will provide with intravenous patient-controlled analgesia device containing morphine for postoperative analgesia

Secondary outcomes

  1. Numerical Rating Scale(NRS)

    Time frame: during postoperative 24 hours

    A numerical rating scale(NRS) requires the patient to rate their pain on defined scale.For example , 0-10 where 0 is no pain and 10 is the worst pain imaginable.

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Registry information

Official study title

Comparison of Erector Spina Plan Block and Rhomboid Intercostal Block for Postoperative Pain Managment in Patients Undergoing Unilateral Breast Surgery

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Dec 20, 2023
Registry last updated
Oct 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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