Skip to main content
MedPathMedPath Home
Clinical Trials/NCT06177665
NCT06177665
Completed
Not Applicable

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

Kocaeli University1 site in 1 country84 target enrollmentJuly 1, 2023
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsPostoperative PainAnalgesia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Kocaeli University
Enrollment
84
Locations
1
Primary Endpoint
Morphin Consumption
Status
Completed
Last Updated
7 months ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

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.

Registry
clinicaltrials.gov
Start Date
July 1, 2023
End Date
June 1, 2024
Last Updated
7 months ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gulnihal Avci

Doctor

Kocaeli University

Eligibility Criteria

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

Outcomes

Primary Outcomes

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

  • Numerical Rating Scale(NRS)(during postoperative 24 hours)

Study Sites (1)

Loading locations...

Similar Trials

Unknown
Not Applicable
Comparison of Erector Spinae Plane Block and Penile Block in Hypospadias SurgeryPostoperative PainAnalgesia
NCT04866368Kocaeli University60
Completed
Not Applicable
Erector Spinae Plane Block Versus Thoracic Paravertebral Block for Pain Control in Modified Radical MastectomyBreast SurgeryThoracic Paravertebral BlockPost-operative Pain ControlErector Spinae Plane BlockOpioid Use
NCT04457115AUSL Romagna Rimini78
Completed
Not Applicable
Erector Spinae Versus Paravertebral in Pediatric PCNLRenal StonePercutaneousNephrolithotomy
NCT05589649Assiut University56
Unknown
Not Applicable
Ultrasound Guided Erector Spinae Plane Block Versus Quadratus Lumborum Block in Laparoscopic CholecystectomyLaparoscopic CholecystectomyPostoperative AnalgesiaErector Spinae Plane BlockQuadratus Lumborum Block
NCT04845711Tanta University60
Unknown
Not Applicable
Comparison of Erector Spinae Plane Block and Pectoral Nerve Block for Acute and Chronic Pain in MastectomiesAcute PainChronic PainMastectomy
NCT05069805Hospital de Base92