Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT04640896

Trigger Point Injections in Anterior Cervical Surgery

Led by George Washington University · Updated on 2022-12-08

60

Participants Needed

1

Research Sites

164 weeks

Total Duration

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AI-Summary

What this Trial Is About

To achieve appropriate exposure for an anterior neck surgery (for example an Anterior Cervical Discectomy and Fusion or ACDF), patients are positioned supine with their neck extended. Due to being in this position, patients frequently complain of posterior neck stiffness and pain postoperatively in addition to the anterior incisional pain. This posterior cervical pain can be classified as myofascial pain. Cervical myofascial pain is thought to be the result of overuse or trauma to the supporting muscles of the neck and shoulders. Trigger point injections are one of the methods used to treat myofascial pain. The trigger point injection procedure is where a physician (typically an anesthesiologist) performs an exam of the patient neck and upper back and finds areas of point tenderness. The physician will then inject a small amount of numbing medication (such as bupivacaine) into the muscle or tissue in that area. Trigger point injections have been shown to be superior to botox injections or dry needling, and equivalent to physical therapy. However, these studies were performed on patients with chronic neck pain. There are no studies evaluating the effectiveness of trigger point injections on post anterior cervical surgery patients. At our institution, trigger point injections with local anesthetic are used as part of a multimodal pain control regimen for post-anterior cervical surgery patients. Our hypothesis is if the addition of trigger point injections to standard of care multi-modal post-operative pain control will decrease patients' myofascial pain, and thereby decrease the amount of narcotic pain medication used.

CONDITIONS

Official Title

Trigger Point Injections in Anterior Cervical Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Elective anterior cervical surgery
Not Eligible

You will not qualify if you...

  • Emergency surgery
  • Allergy to local anesthetics
  • Long-term opioid use (excluding tramadol and codeine)
  • Complications during surgery such as unstable cervical spine

AI-Screening

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Trial Site Locations

Total: 1 location

1

George Washington University Hospital

Washington D.C., District of Columbia, United States, 20037

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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