Erector Spinae Plane Block For Lumbar Disc Hernia Repair

Postoperative Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03744689
• Other study ID #: KIA2018/440
• Status: Completed
• Phase: N/A
• Start date: October 1, 2019
• Est. completion date: February 4, 2020

Study information

• Verified date: February 2020
• Source: Kocaeli University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: February 4, 2020
• Est. primary completion date: February 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Hernia
• Pain, Postoperative
• Postoperative Pain

Intervention

Procedure:
• Erector Spinae Plane block
Erector Spinae plane block will be done according to hernia level using bupivacaine hydrochloride
• Sham block
Sham block will be done with serum physiologic.

Drug:
• Bupivacaine Hydrochloride
20 ml 0,25% Bupivacaine will be used for block performances

Device:
• PCA
Intravenous morphine patient controlled analgesia device will be given to the patients postoperatively and 24 hour morphine consumption will be recorded

Locations

Country	Name	City	State
Turkey	Kocaeli University	Kocaeli

Sponsors (1)

Lead Sponsor	Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Morphine consumption	morphine consumptions will be recorded	postoperative first 24 hour
Secondary	Numeric rating scale	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.	postoperative first 24 hour