A Multi-center, Randomized, Placebo-controlled, Double-blind, Cross-over, Phase 3 Clinical Trial to Evaluate of the Efficacy and Safety of DW9801 in Patients with Primary Dysmenorrhea
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
120
Pelubiprofen 45mg 1 tab for moderate or severe menstrual pain, bid for 3days(prn)
Placebo1 tab for moderate or severe menstrual pain, bid for 3days(prn)
TOTPAR-8
Time weighted sum of total pain relief
Time frame: Day 1
SPID-8
Sum of pain intensity difference
Time frame: Day 1
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