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

Not Applicable

Completed

• Conditions: Postoperative Pain; Analgesia
• Interventions: Other: Rhomboid Intercostal Block; Other: Erector Spinae Plane Block

• Registration Number: NCT06177665
• Lead Sponsor: Kocaeli University

Brief Summary

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.

Detailed Description

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.

Study Timeline

• Study Start: 2023-07-01
• Study First Submitted: 2023-12-11
• Study First Submitted QC: 2023-12-11
• Study First Posted: 2023-12-20
• Primary Completion: 2024-03-30
• Study Completion: 2024-06-01
• Status Verified: 2024-07
• Last Update Submitted: 2024-07-17
• Last Update Posted: 2024-07-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 84

Inclusion Criteria

Not provided

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Rhomboid Intercostal Block	Rhomboid Intercostal Block	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.
Erector Spinae Plane Block	Erector Spinae Plane Block	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.

Primary Outcome Measures

Name	Time	Method
Morphin Consumption	during postoperative 24 hours	Patients in both groups will provide with intravenous patient-controlled analgesia device containing morphine for postoperative analgesia

Secondary Outcome Measures

Name	Time	Method
Numerical Rating Scale(NRS)	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.

Trial Locations

Locations (1)

Kocaeli University; 🇹🇷 Kocaeli, Turkey