Erector Spinae Plane Block in Spine Surgeries (ESB)

Ain Shams University

Status and phase: Unknown; Phase 4

Conditions: Lumbar Disc Disease

Treatments: Procedure: erector spinae block for group E

Study type: Interventional

Funder types: Other

Identifiers

NCT05247021

ainshmas university

Details and patient eligibility

About

Aim of this study was to assess the efficacy of erector spinae plane block (ESB) for postoperative pain management in lumbar spine surgery.

Enrollment: 44 estimated patients

Sex: All

Ages: 20 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients American Society of Anesthesiologists physical status (ASA) I and II.
• Both sexes.
• Age between 20 to 60 years old.
• Scheduled for lumbar spine surgeries.

Exclusion criteria

• Patients who received long acting opioids preoperatively.
• Patients with bleeding disorders and coagulopathy.
• Infection at the injection site.
• Allergy to local anesthetics.
• Patients with significant cognitive dysfunction.
• Patients with diabetic neuropathy.
• Patients with uncontrolled hypertension or diabetes.
• Patients with advanced cardiac, respiratory, hepatic or renal disease.
• Patients with viral hepatitis or HIV.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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44 participants in 2 patient groups

erector spinae block group (E)

Experimental group

Description:

patients will receive bilateral ultrasound guided erector spinae block before the lumbar spine surgery starts.(20ml of bupivacaine 0.25%) after receiving general anesthesia

Treatment:

Procedure: erector spinae block for group E

control group (C)

No Intervention group

Description:

patients will receive standard general anesthesia for lumbar spine surgery according to hospital protocol.