The purpose of this clinical study is to determine whether or not DW-1030 is not inferior to eperisone HCl in efficacy and safety.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
242
Changes of Finger-to-Floor Distance(FFD) compared to baseline 7days after administration
Time frame: 1, 3, 7 day
Changes of 100mm Pain VAS
Time frame: -3, 1, 3, 7 day
Oswestry Disability Index (ODI)
Time frame: 1, 3, 7 day
Physician's Global Assessment
Time frame: 7 day
The number of using rescue drugs and the total amount
Time frame: 1, 3, 7 days
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