一小段医学方面的英文翻译成中文,非常感谢!

一小段医学方面的英文翻译成中文,非常感谢!There were 3 primary efficacy variables evaluated in this trial:patient self- assessment of magnitude of pain via a 100 mm visual analog scale(VAS), patient self- assessment of pain relief via a categorical relief scale(0-5), and investigator's sensory skin testing (allodynia). QuantitativeThermal Sensory Testing (QST) was done on select patients at the discretion ofthe investigators for investigational research purposes.Safety was evaluatedvia the following: monitoring of systemic lidocaine blood levels following 6hours of patch-use, patient's self-reporting of symptoms via a 27-itemside-effects check list, and skin examinations of the area treated.The Sponsor analyzed the trial data using atwo-way analysis of variance controlling for treatment and investigationalsite forthe following studyefficacy variables: VAS painreduction (Sessions 1 and 2), pain relief (Sessions 1, 2 and 3),VAS painreduction during home use (days 1 to 21), and allodynia testing (sessions 1 and2). The Sponsor also looked at data from the 7-day washout period collectedfrom patients who opted to participate in the open-label continuous useextension.