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OpenTrials
Completed

NCT Number: NCT07652177

Comparison of the Analgesic Efficacy of Erector Spinae Plane Block in Lumbar Microdiscectomy Surgeries

Comparison of the Analgesic Efficacy of Lumbar Erector Spinae Plane Block and Sacral Erector Spinae Plane Block in Lumbar Microdiscectomy Surgeries

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Key information

About this study

Postoperative pain is commonly observed in patients undergoing lumbar microdiscectomy surgery.

To manage this pain, the lumbar erector spinae plane (ESP) block is frequently administered as part of a multimodal analgesia regimen, particularly with the aim of reducing opioid consumption in these patients.

Recent publications have demonstrated the analgesic efficacy of the sacral erector spinae plane block in lumbar microdiscectomy surgeries.

In this study, the postoperative analgesic effectiveness of the lumbar ESP block-performed two vertebral levels above the surgical site-will be compared with that of the sacral ESP block-performed two vertebral levels below the surgical site.

It is anticipated that this approach will provide effective analgesia while avoiding the use of opioids.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

ASA I, ASA II, and ASA III patients scheduled for single-level lumbar microdiscectomy at the L4-L5 or L5-S1 level.

Exclusion criteria

Pregnant patients

Patients who do not consent to the erector spinae plane block

Patients requiring mechanical ventilatory support

Patients with a history of substance abuse

Patients with a known allergy to the medications to be used

Patients with bleeding diathesis

Patients with infection at the planned block site

Patients undergoing surgical intervention at two or more spinal levels

Patients with communication difficulties or intellectual disabilities

Patients with neuropsychiatric disorders

Patients with chronic pain

Patients with an expected surgical duration of 180 minutes or more

Patients with a prior history of lumbar microdiscectomy

Treatment and study plan

Primary outcomes

  1. total tramadol consumption

    Time frame: first 24 hours after the surgery

Secondary outcomes

  1. patients' visual analog scale

    Time frame: first 24 hours after the surgery

    To compare postoperative Visual Analog Scale (VAS) pain scores at 2, 4, 8, 12, and 24 hours.

  2. To compare analgesic consumption during the postoperative time intervals of 0-2, 2-4, 4-8, 8-12, and 12-24 hours.

    Time frame: first 24 hours after the surgery

    postoperative 0-2, 2-4, 4-8, 8-12, and 12-24 hours.

Sponsors and collaborators

Lead sponsor

Gaziosmanpasa Research and Education Hospital

Other Gov

Registry information

Official study title

Comparison of the Analgesic Efficacy of Lumbar Erector Spinae Plane Block and Sacral Erector Spinae Plane Block in Lumbar Microdiscectomy Surgeries

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 16, 2026
Registry last updated
Jun 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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