To determine the efficacy of lidocaine injection of trigger points versus subcutaneous injection in patients with subacute whiplash associated disorder following injury.
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 Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Department of physical medicine and rehabilitation, McMaster University
Hamilton, Ontario, Canada
HHS (Juravinski Hospital Site)
Hamilton, Ontario, Canada
pain
10 cm Visual Analog Scale
Time frame: 2 weeks following injection
cervical range of motion
Time frame: Immediately, 2 and 6 weeks after injection
self-report neck disability
Time frame: Immediately, 2 and 6 weeks after injection
globe perceived effects
The Short Form-12
Time frame: Immediately, 2 and 6 weeks after injection
work performance
questionnaire
Time frame: Immediately, 2 and 6 weeks after injection
pain
10 cm Visual Analog Scale
Time frame: 5 minutes following injection
pain
10 cm Visual Analog Scale
Time frame: 6 weeks following injection
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