Stopped: Main researcher (Jonathan Lee) left the institution. Once he left, recruitment did not occur.
The aim of this trial is to investigate the efficacy of trigger point injections with 1% lidocaine in reducing myofascial back and neck pain in the Emergency Department compared to lidocaine patches 5%.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
absolute change in Numerical Rating Scale (NRS) of pain
Timeframe: 0 minutes and 20-minutes post- treatment, and every 30-60 minutes thereafter until discharge or admission and we will give the patient a hand out so that they can record their pain scores for up to 5 days after their emergency department visit.