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Efficacy of propiverine ER with or without α-blockers related to maximum urinary flow rate in adult men with OAB: results of a 12-week multicenter non-interventional study

机译：有或没有α-阻滞剂的普罗普利汀ER的疗效与OAB成年男性最大尿流率有关：一项为期12周的多中心非干预性研究的结果

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摘要

PurposeComparison of efficacy of propiverine extended release (ER) 30 mg o.d. in the treatment of male OAB administered as monotherapy (MT) or add-on to α-blockers (combination treatment, CT) in relation to maximum urinary flow (Qmax) in a non-interventional study.

机译：目的比较普罗维林缓释剂（ER）30 mg.o.d的疗效。在一项非介入性研究中，以单药疗法（MT）或与α-受体阻滞剂联合使用的男性OAB治疗（联合治疗，CT）与最大尿流量（Qmax）有关。

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期刊名称 Springer Open Choice
作者
Matthias Oelke; Sandra Murgas; Ina Baumann; Frieder Schnabel; Martin C. Michel;
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作者单位

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年(卷),期 -1(29),2
年度 -1
页码 217–223
总页数 7
原文格式 PDF
正文语种
中图分类外科学;
关键词
Lower urinary tract symptoms Overactive bladder syndrome Cholinergic antagonists Adrenergic α-antagonists Urinary retention Propiverine hydrochloride;

机译：下尿路症状;膀胱过度活动症候群;胆碱能拮抗剂;肾上腺素能α-拮抗剂;尿retention留;盐酸丙哌维林;

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1. Efficacy of propiverine ER with or without alpha-blockers related to maximum urinary flow rate in adult men with OAB: results of a 12-week, multicenter, non-interventional study. [J] . Oelke M, Murgas S, Baumann I, World journal of urology . 2011,第2期

机译：在患有OAB的成年男性中，有或没有α受体阻滞剂与普罗布林ER的功效与最大尿流率有关：一项为期12周的多中心非干预性研究的结果。
2. Efficacy of propiverine ER with or without α-blockers related to maximum urinary flow rate in adult men with OAB: results of a 12-week, multicenter, non-interventional study [J] . Matthias Oelke, Sandra Murgas, Ina Baumann, World Journal of Urology . 2011,第2期

机译：有或没有α-阻滞剂的普罗普利汀ER的疗效与OAB成年男性最大尿流率有关：一项为期12周的多中心非干预性研究的结果
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7. Efficacy of propiverine ER with or without α-blockers related to maximum urinary flow rate in adult men with OAB: results of a 12-week, multicenter, non-interventional study [O] . Matthias Oelke, Sandra Murgas, Ina Baumann, 2011

机译：有或没有α-阻滞剂的普罗普利汀ER的疗效与OAB成年男性最大尿流率有关：一项为期12周的多中心非干预性研究的结果

Efficacy of propiverine ER with or without α-blockers related to maximum urinary flow rate in adult men with OAB: results of a 12-week multicenter non-interventional study

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