Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT04646707

Effect of Erector Spinae (ESP) Block on Opioid Reduction and Enhanced Recovery After Posterior Cervical Spine Surgery

Led by University Health Network, Toronto · Updated on 2025-01-30

52

Participants Needed

1

Research Sites

306 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients undergoing spine surgery frequently experience significant pain after surgery. This can limit patient activity and hinder rehabilitation. If inadequately treated, severe pain can result in emotional and psychological distress and ultimately impact long-term function, and increase the risk of developing pain that lasts longer than six months associated with depression, anxiety and disability. More specifically, Erector Spinae Plane (ESP) block is a recently described plane block designed to block the dorsal and ventral rami of the thoracic spinal nerves. It has shown to be an effective modality for postoperative pain management as a part of multimodal analgesia in spinal surgery.

CONDITIONS

Official Title

Effect of Erector Spinae (ESP) Block on Opioid Reduction and Enhanced Recovery After Posterior Cervical Spine Surgery

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 80 years
  • ASA class I to III
  • Undergoing posterior cervical (C3-T2) decompression and instrumented fusion for cervical stenosis
  • Surgery performed in prone position
Not Eligible

You will not qualify if you...

  • Allergy to local anesthetics
  • ASA class IV
  • Lack of informed consent
  • Pregnancy
  • Cervical spine fracture
  • Extradural or intradural cervical tumors
  • Surgery involving C1 and C2 spine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Toronto Western Hospital?UHN

Toronto, Ontario, Canada, M5T 2S8

Actively Recruiting

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Research Team

M

Michael Dinsmore, MD

CONTACT

K

Ki Jinn Chin, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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