Comparison of the Postoperative Analgesic Efficacy of Classical and Modified Erector Spinae Plane Blocks After Lumbar Spinal Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorSamsun University

About this trial

The investigators aim to compare the postoperative analgesic efficacy of the classical erector spinae plane block and the modified erector spinae plane block in the management of postoperative analgesia after lumbar disc surgery.

Eligibility criteria

Qualifiers

Patients aged 18-70 years,

Classified as ASA physical status I-III,

Scheduled to undergo single-level lumbar spinal surgery under general anesthesia

Who agree to participate in the study by providing written informed consent

Disqualifiers

History of bleeding diathesis or current anticoagulant therapy

Known allergy or hypersensitivity to local anesthetics or opioid medications

Infection at the planned block injection site

Previous lumbar spine surgery

Trial design

Treatments tested in this trial

  • The Classical Erector Spinae Plane Block
  • Modified Erector Spinae Plane Blocks

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators