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Clinical Effect Of Shuniao Granule In Treating Female Urethral Syndrome (FUS)

Posted on:2019-07-02Degree:MasterType:Thesis
Country:ChinaCandidate:S S YangFull Text:PDF
GTID:2394330545472691Subject:Integrative Medicine
Abstract/Summary:PDF Full Text Request
Objective:To observe the clinical efficacy of Shuniao granules in the treatment of female urethral syndrome(FUS).METHODS:A total of 72 women with urethral syndrome(FUS)who met the inclusion criteria were selected from the Department of Urology,the First Affiliated Hospital of Heilongjiang University of Chinese Medicine.They were randomly divided into two groups.In the treatment group,36 patients took a granule of Shuniao Granule with warm water,2 times a day.36 cases in the control group were treated with oral Yinhuamiyanling tablets,4 tablets at a time,4 times a day.The course of treatment for both groups was 2 weeks(14 days).I-PSS before and after treatment for both groups of patients Questionnaires,QOL,residual urine volume,maximum urinary flow rate,and clinical symptoms were statistically analyzed.Results:The therapeutic effect of the treatment group and control group after treatment was better than before treatment.The scores of I-PSS questionnaire,QOL,Qmax,and single symptoms of traditional Chinese medicine were significantly improved after treatment in both groups,and theI-PSS questionnaire score and Qmax before and after treatment were statistically significant(P<0.05).The frequency of urination in the TCM symptom scores and the symptoms of weakness in the waist and knee were significantly different between the treatment group and the control group(P<0.05).There was no significant difference in residual urine volume after treatment between the two groups(P>0.05).Conclusion:Shuniao granule can effectively treat female urethral syndrome,significantly improve urinary storage symptoms,micturition symptoms and post-void symptoms,improve the quality of life of patients,and no adverse reactions.
Keywords/Search Tags:Female urinary tract syndrome, Shuniao granule, Clinical efficacy observation
PDF Full Text Request
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