This is a randomized, double-blind, placebo-controlled study designed to assess the efficacy and safety of 5% lidocaine patch, following placebo or active patch applications in placebo insensitive subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
243
5% Lidocaine patch to be placed on the site of pain
Placebo patch to be placed on the site of pain
Beijing University People's Hospital
Beijing, Beijing Municipality, China
Air force general hospital
Beijing, China
Change of VAS score
Mean change in the mean pain VAS score
Time frame: over 24 hour from baseline to the post-treatment over time during double-blind period
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...and 11 more locations