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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorAnkara Etlik City Hospital

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Patients with chronic pain conditions

Patients with a history of chronic opioid use

Patients undergoing emergency lumbar stabilization surgery

Trial design

Treatments tested in this trial

  • Single-Level Erector Spinae Plane Block
  • Two-Level Erector Spinae Plane Block

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators