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Erector Spinae Plane Block For Lumbar Disc Hernia Repair

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03744689
Enrollment
60
Registered
2018-11-16
Start date
2019-10-01
Completion date
2020-02-04
Last updated
2020-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

Lomber disc hernia, Erector spinae plane block, Postoperative pain

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.

Interventions

PROCEDUREErector Spinae Plane block

Erector Spinae plane block will be done according to hernia level using bupivacaine hydrochloride

PROCEDURESham block

Sham block will be done with serum physiologic.

DRUGBupivacaine Hydrochloride

20 ml 0,25% Bupivacaine will be used for block performances

DEVICEPCA

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

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Morphine consumptionpostoperative first 24 hourmorphine consumptions will be recorded

Secondary

MeasureTime frameDescription
Numeric rating scalepostoperative first 24 hourNumeric 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026