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7% study completion price) had been able to tolerate the study medication well. The tramadol twenty five mg was observed to not be statistically significantly distinctive from placebo in the main Assessment (SPID48), and therefore formal testing of The true secret secondary findings wasn't performed for tramadol twenty five mg, in accordance with

Common patient international assessment at scheduled time factors was assessed for treatment group differences applying an ANCOVA with pooled study Middle along with the baseline pain rating as covariates. Full use of rescue medication was calculated as the overall amount of rescue analgesia (mg) captured while in the rescue medications Digital cir