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Clinical Trial Summary

To determine the efficacy of lidocaine injection of trigger points versus subcutaneous injection in patients with subacute whiplash associated disorder following injury.


Clinical Trial Description

This is a double-blind, randomized controlled trial to determine the efficacy of lidocaine injection of trigger points versus subcutaneous injection in patients with subacute whiplash associated disorder following injury. Outcomes include pain, objective assessment, self-report function recovery, impact on work performance and globe perceived effects which will be assessed 5 minutes, 2 and 6 weeks following injection. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02060734
Study type Interventional
Source Hamilton Health Sciences Corporation
Contact
Status Withdrawn
Phase Phase 4
Start date October 2015
Completion date September 2016

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