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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • The Classical Erector Spinae Plane Block

    Other intervention

    The erector spinae plane block will be performed under ultrasound guidance before the induction of general anesthesia.

  • Modified Erector Spinae Plane Blocks

    Other intervention

    Modified erector spinae plane blocks will be performed under ultrasound guidance before the induction of general anesthesia.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Active Comparator: Group K-ESPActive comparator 1 intervention
Group B: Active Comparator: Group M-ESPActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Opioid consumption

In the postoperative period, patients will be given opioids according to their pain density with a patient-controlled device, and the daily Morphine consumption in Patient Controlled Analgesia device will be collected and compared between groups.

Time frame
24 hours

Secondary outcomes

1

Perioperative pain intensity

Changes in the Numerical Rating Scale (NRS) will be recorded at rest and during movement. The participant's baseline NRS will be recorded, followed by measurements before and after neuraxial positioning and up to 24 hours post-surgery. The NRS is a unidimensional measure of pain intensity in adults. It is a segmented numerical version of the Visual Analog Scale (VAS) where the participant selects a whole number (0-10) that best represents the intensity of their pain. The 11-point numerical scale ranges from '0' representing one end of the pain spectrum (e.g. 'no pain') to '10' representing the other end (e.g. 'worst imaginable pain').

Time frame
24 hours
2

Quality of recovery 15 scale

Postoperative Quality of Recovery 15 in Turkish scale

Time frame
24 hours after surgery
3

Postoperative nausea and vomiting

Postoperative nausea and vomiting (PONV): During follow-up, patients who experience nausea or vomiting will be evaluated using a verbal descriptive PONV scale (0=None, 1=Mild nausea, 2=Moderate nausea, 3=Single episode of vomiting, 4=More than one episode of vomiting).

Time frame
24 hours

Other outcomes

Sponsors and contacts

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