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

Recruiting N/A Interventional Study
Postoperative Pain
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
52 (estimated)
Sponsor
University Health Network, Toronto · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
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 disabili…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: All adult patients aged 18-80 years with ASA class I - III undergoing posterior cervical (C3-T2) decompression and instrumented fusion for cervical stenosis in prone position. Exclusion Criteria: 1. In patients who are allergic to local anesthetics. 2. ASA IV patients 3. Lack …
Contacts

Michael Dinsmore, MD

416 603 5800

michael.dinsmore@uhn.ca

CONTACT

Ki Jinn Chin, MD

416 603 5800

CONTACT