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Clinical Trials/NCT03744689
NCT03744689
Completed
Not Applicable

The Effect Of Erector Spinae Plane Block On Postoperative Pain Management In Lumbar Disc Hernia Repair Operation

Kocaeli University1 site in 1 country60 target enrollmentOctober 1, 2019

Overview

Phase
Not Applicable
Intervention
Erector Spinae Plane block
Conditions
Postoperative Pain
Sponsor
Kocaeli University
Enrollment
60
Locations
1
Primary Endpoint
Morphine consumption
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Pain management after lomber disc hernia repair surgery is a challenging issue for anesthetists. Erector Spinae plane block is a novel analgesic technique which could be used for this purpose. Primary aim of this double blinded randomized controlled study is to compare the analgesic efficacy of this new block technique with control group in this group of patients.

Registry
clinicaltrials.gov
Start Date
October 1, 2019
End Date
February 4, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dilek İçli

Associate professor

Kocaeli University

Eligibility Criteria

Inclusion Criteria

  • Age 18-65 years
  • Undergoing elective lomber disc hernia

Exclusion Criteria

  • ASA III - IV
  • infection of the skin at the site of needle puncture area
  • patients with known allergies to any of the study drugs
  • coagulopathy

Arms & Interventions

Erector Spinae Plane Block

Erector Spinae Plane Block Group Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks

Intervention: Erector Spinae Plane block

Erector Spinae Plane Block

Erector Spinae Plane Block Group Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks

Intervention: Bupivacaine Hydrochloride

Erector Spinae Plane Block

Erector Spinae Plane Block Group Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks

Intervention: PCA

Control Group

Sham block will be done with serum physiologic.

Intervention: Sham block

Control Group

Sham block will be done with serum physiologic.

Intervention: PCA

Outcomes

Primary Outcomes

Morphine consumption

Time Frame: postoperative first 24 hour

morphine consumptions will be recorded

Secondary Outcomes

  • Numeric rating scale(postoperative first 24 hour)

Study Sites (1)

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