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Effect of electroacupuncture versus pelvic floor muscle training plus solifenacin for moderate and severe mixed urinary incontinence in women: a study protocol

机译:电针对骨盆底肌训练联合索非那新治疗中重度混合性尿失禁的疗效研究方案。

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Background In women with mixed urinary incontinence, pelvic floor muscle training and solifenacin is the recommended conservative treatment, while electroacupuncture is a safe, economical and effective option. Methods/Design In this prospective, multi-center, randomized controlled trial, five hundred women with mixed urinary incontinence, from 10 centers will be randomized to receive either electroacupuncture or pelvic floor muscle training plus solifenacin. Women in the acupuncture group will receive electroacupuncture for 3 sessions per week, over 12 weeks, while women in the control group will receive pelvic floor muscle training plus solifenacin (5 mg once daily) for 36 weeks. The primary outcome measure is the proportion of change in 72-hour incontinence episode frequency from baseline to week 12. The secondary outcome measures include eleven items, including proportion of participants with ≥50% decrease in average 72-h incontinence episode frequency, change from baseline in the amount of urine leakage and proportion of change from baseline in 72-h incontinence episode frequency in week 25–36, and so forth. Statistical analysis will include covariance analysis, nonparametric tests and t tests. Discussion The objective of this trial is to compare the efficacy and safety of electroacupuncture versus pelvic floor muscle training plus solifenacin in women with moderate and severe mixed urinary incontinence. Trial registration ClinicalTrials.gov Identifier: NCT02047032
机译:背景技术对于混合性尿失禁的女性,建议进行骨盆底肌肉训练和索非那新作为保守治疗,而电针疗法是一种安全,经济和有效的选择。方法/设计在这项前瞻性,多中心,随机对照试验中,将对来自10个中心的500名混合性尿失禁的妇女进行随机分配,以接受电针或骨盆底肌肉训练加索非那新治疗。针灸组的妇女将在12周内每周接受3次电针疗法,而对照组的妇女将接受36周的骨盆底肌肉训练和索非那新(每天5 mg)训练。主要结局指标是从基线到第12周的72小时失禁发作频率变化的比例。次要结局指标包括11个项目,包括平均72小时失禁发作频率降低≥50%的参与者比例,尿液漏出量的基线以及在25-36周内72小时失禁发作频率与基线相比变化的比例,等等。统计分析将包括协方差分析,非参数检验和t检验。讨论本试验的目的是比较电针和骨盆底肌肉训练加索非那新在中度和重度混合性尿失禁妇女中的疗效和安全性。试验注册ClinicalTrials.gov标识符:NCT02047032

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