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Not yet recruiting NCT07363096

Single- Versus Two-Level ESP Block for Analgesia After Lumbar Stabilization Surgery

No phase Interventional Postoperative Pain Management Lumbar Spinal Fusion Surgery Erector Spina Plan Block

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Single-Level Erector Spinae Plane Block, Two-Level Erector Spinae Plane Block.
Who it may be relevant to
Registry conditions: Postoperative Pain Management, Lumbar Spinal Fusion Surgery, Erector Spina Plan Block. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison Of Single- Versus Two-Level Erector Spinae Plane Block For Postoperative Analgesia In Patients Undergoing Lumbar Stabilization Surgery

Overview

Lumbar stabilization surgery is commonly associated with moderate to severe postoperative pain. Effective pain control is important to improve patient comfort, early mobilization, and recovery. The erector spinae plane (ESP) block is a regional anesthesia technique that has been increasingly used for postoperative pain management in spine surgery. This study aims to compare the effectiveness of single-level versus two-level ultrasound-guided ESP block for postoperative pain control in patients undergoing lumbar stabilization surgery. Patients will be randomly assigned to receive either a single-level ESP block or a two-level ESP block in addition to standard analgesic treatment. Postoperative pain scores, opioid consumption, and the incidence of side effects will be evaluated during the postoperative period. The results of this study may help determine the most effective ESP block technique for pain management after lumbar stabilization surgery.

Interventions

  • Procedure Single-Level Erector Spinae Plane Block
    Ultrasound-guided erector spinae plane block performed at a single vertebral level for postoperative analgesia.
  • Procedure Two-Level Erector Spinae Plane Block
    Ultrasound-guided erector spinae plane block performed at two adjacent vertebral levels for postoperative analgesia.

Primary outcome measures

  • Intraoperative Remifentanyl Consumption [Time frame: During the intraoperative period]
Secondary outcome measures (1)
  • Pain Scores [Time frame: First 24 hours after surgery]

Eligibility criteria

Inclusion criteria

  • ASA I-II-III,
  • BMI:18-40,
  • Patients undergoing lumbar stabilization surgery involving 2 to 4 vertebral levels
  • Patients who personally provide written informed consent to participate in the study

Exclusion criteria

  • Patients with chronic pain conditions
  • Patients with a history of chronic opioid use
  • Patients undergoing emergency lumbar stabilization surgery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Ankara Etlik City Hospital — Ankara

Identifiers

NCT: NCT07363096 · AEŞH-EK1-2023-250

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗