Erector Spinae Plane Block in Spine Surgeries

Phase 4

• Conditions: Lumbar Disc Disease
• Interventions: Procedure: erector spinae block for group E

• Registration Number: NCT05247021
• Lead Sponsor: Ain Shams University

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2021-01-22
• Status Verified: 2021-12
• Study First Submitted: 2022-01-11
• Study First Submitted QC: 2022-02-09
• Last Update Submitted: 2022-02-09
• Study First Posted: 2022-02-18
• Last Update Posted: 2022-02-18
• Primary Completion: 2022-04-22
• Study Completion: 2022-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 44

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.

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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.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

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

Primary Outcome Measures

Name	Time	Method
the postoperative 24 hours morphine consumption	24 hours postoperative	the analgesic effect of erector spine block will be assessed postoperative by numeric rating scale (NRS), if NRS is more than 3 the patient will receive a rescue dose of 5 milligrams of morphine

Secondary Outcome Measures

Name	Time	Method
Mean Blood pressure in mmHg	24 hours postoperative	Measure mean blood pressure of patients postoperative every 4 hours
First time of mobilization to a chair	24 hours postoperative	Measure the time to first mobilization to a chair in minutes
Patient satisfaction	24 hours postoperative	Measure patient satisfaction by asking the patient if he is satisfied or not " yes or no"
Heart rate	24 hours postoperative	Measure heart of the patients postoperative every 4 hours

Trial Locations

Locations (1)

Ain Shams University; 🇪🇬 Cairo, Egypt