Edge of Laminar Block Versus Erector Spinae Plane Block for Postoperative Analgesia in Video-Assisted Thoracoscopic Surgery

NCT ID: NCT07201285

Last Updated: 2025-10-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-10-01

Study Completion Date

2026-04-01

Brief Summary

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This study aims to compare the ultrasound-guided edge of laminar block (ELB) and erector spinae plane block (ESPB) for postoperative analgesia in patients undergoing video-assisted thoracic surgery (VATS).

Detailed Description

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Postoperative pain after thoracic surgery, which is attributed to muscle incisions, rib retractions, and intercostal nerve damage, may be severe enough to cause pulmonary complications, such as atelectasis, pneumonia, and increased oxygen consumption.

The erector spinae plane block (ESPB) is used for managing post-thoracotomy pain and has numerous advantages that make it an attractive alternative technique. The ESPB injects a local anaesthetic around the erector spinae muscle at approximately the level of the T5. It may be able to block the dorsal and ventral rami of the thoracic spinal nerves.

A novel technique of retrolaminar block (RLB) called the edge of laminar block (ELB) to provide sensory analgesia during rib fracture surgery.

Conditions

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Edge of Laminar Block Erector Spinae Plane Block Postoperative Analgesia Video-Assisted Thoracoscopic Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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ELB group

Patients will receive edge of laminar block using 20ml of bupivacaine 0.25%.

Group Type EXPERIMENTAL

Edge of laminar block

Intervention Type OTHER

Patients will receive edge of laminar block using 20ml of bupivacaine 0.25%.

ESPB group

Patients will receive an erector spinae plane block using 20ml of bupivacaine 0.25%.

Group Type EXPERIMENTAL

Erector spinae plane block

Intervention Type OTHER

Patients will receive an erector spinae plane block using 20ml of bupivacaine 0.25%.

Interventions

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Edge of laminar block

Patients will receive edge of laminar block using 20ml of bupivacaine 0.25%.

Intervention Type OTHER

Erector spinae plane block

Patients will receive an erector spinae plane block using 20ml of bupivacaine 0.25%.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age from 18 to 65 years.
* Both sexes.
* American Society of Anesthesiology (ASA) physical status I-II.
* Undergoing video-assisted thoracic surgery (VATS) under general anesthesia.

Exclusion Criteria

* History of allergies to local anesthetics.
* Opioid dependency.
* Bleeding or coagulation disorders.
* Psychiatric and neurological disorder.
* Local infection at the site of injection.
* Severe heart, lung, liver, and renal dysfunction.
* Pregnant or lactating women.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tanta University

OTHER

Sponsor Role lead

Responsible Party

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Mohammed Said ElSharkawy

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Tanta University

Tanta, El-Gharbia, Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Mohammed S Elsharkawy, MD

Role: CONTACT

00201148207870

Facility Contacts

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Mohammed S Elsharkawy, MD

Role: primary

00201148207870

Other Identifiers

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36264PR1336/8/25

Identifier Type: -

Identifier Source: org_study_id

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