Erector Spinae Plane Block For Lumbar Disc Hernia Repair

Not Applicable

Completed

• Conditions: Postoperative Pain
• Interventions: Procedure: Erector Spinae Plane block; Procedure: Sham block; Drug: Bupivacaine Hydrochloride; Device: PCA

• Registration Number: NCT03744689
• Lead Sponsor: Kocaeli University

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2018-11-15
• Study First Submitted QC: 2018-11-15
• Study First Posted: 2018-11-16
• Study Start: 2019-10-01
• Status Verified: 2020-02
• Primary Completion: 2020-02-01
• Study Completion: 2020-02-04
• Last Update Submitted: 2020-02-04
• Last Update Posted: 2020-02-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• ASA I-II
• Age 18-65 years
• Undergoing elective lomber disc hernia

Exclusion Criteria

• obesity
• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
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
Erector Spinae Plane Block	Bupivacaine Hydrochloride	Erector Spinae Plane Block Group Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks
Erector Spinae Plane Block	PCA	Erector Spinae Plane Block Group Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks
Control Group	Sham block	Sham block will be done with serum physiologic.
Control Group	PCA	Sham block will be done with serum physiologic.

Primary Outcome Measures

Name	Time	Method
Morphine consumption	postoperative first 24 hour	morphine consumptions will be recorded

Secondary Outcome Measures

Name	Time	Method
Numeric rating scale	postoperative first 24 hour	Numeric rating scale for pain will be used for pain evaluation. The scale is scored in a range of 0-10 with 0 representing no pain 10 representing the highest degree of pain.

Trial Locations

Locations (1)

Kocaeli University; 🇹🇷 Kocaeli, Turkey