Overview

Adjunctive 5% Lidocaine Patches for Acute Non-radicular Low Back Pain in Emergency Department Patients

Status:
Unknown status
Trial end date:
2020-07-01
Target enrollment:
0
Participant gender:
All
Summary
This study will evaluate the addition of lidocaine % transdermal patches to standard therapy in the treatment of acute non-radicular low back pain in patients discharged from the Emergency Department. In addition to standard therapy, half of the participants will receive medicated patches while the other half will receive non-medicated patches.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
John H. Stroger Hospital
Treatments:
Lidocaine
Criteria
Inclusion Criteria:

- pain originating between the lower border of the scapulae and the upper gluteal folds

- treating ED physician plan for discharge of the patient

Exclusion Criteria:

- radicular pain defined as pain radiating below the gluteal folds

- direct trauma to the back within previous month

- pain of greater than 2 weeks duration or greater than 1 LBP episode per month in the
past 3 months

- patient being pregnant or lactating; no access to phone or ability to participate in
follow-up phone calls

- known allergy to lidocaine or skin breakdown over site of pain

- treating physician plan for opioid prescription (tramadol, codeine, hydrocodone)

- personal history of malignancy, fever (temperature greater than 37.9ÂșC), or previous
spinal surgery

- patients who are detainees

- previous enrollment in the study