Actively Recruiting

Phase 4
Age: 18Years +
All Genders
ID04640896

Comparison of Trigger Point Injections Versus Traditional Therapies in the Management of Postsurgical Pain in Patients Who Had Anterior Cervical Surgery

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

60

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the use of trigger point injections to manage pain after anterior cervical surgery, such as Anterior Cervical Discectomy and Fusion (ACDF). This surgery often requires patients to lie on their back with their neck extended, which can cause stiffness and pain in the back of the neck, known as myofascial pain. This pain is believed to result from overuse or injury to neck and shoulder muscles, and while trigger point injections are used for chronic neck pain, their effectiveness after this type of surgery has not been studied. The study compares three approaches: a small skin injection of lidocaine (not a trigger point injection), trigger point injections with normal saline, and trigger point injections with bupivacaine hydrochloride. All injections are given by anesthesiology providers within an hour after surgery using a standardized sterile technique. Participants also receive a standard pain control regimen during and after surgery. The aim is to see if adding trigger point injections reduces pain and narcotic pain medication use. Participants will be monitored for opioid use and pain levels at 6, 12, and 24 hours after the injection. Researchers will also track the length of hospital stay. The study uses a randomized design with single blinding. Overall participation lasts through hospital discharge, typically about two days. Assessments include pain scores and opioid consumption to evaluate if trigger point injections improve pain management after anterior cervical surgery.

CONDITIONS

Brief 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
  • Local anesthetic allergy
  • Long term opioid usage (not including tramadol and codeine)
  • Intra-operative complication (e.g. unstable cervical spine)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 24 hours after surgery

Participants receive trigger point injections or lidocaine skin wheal shortly after anterior cervical surgery to manage postsurgical pain.

1 treatment visit occurring within an hour of arrival to post anesthesia care unit

Post-operative Follow-up

Duration - Through hospital discharge, an average of 2 days

Participants are monitored for pain levels and opioid consumption, with typical hospital stay lasting about 2 days.

Approximately 1 to 2 post-operative visits during hospital stay

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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