首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >A 52‐week multicenter randomized controlled study of the efficacy and safety of add‐on dutasteride and imidafenacin to tamsulosin in patients with benign prostatic hyperplasia with remaining overactive bladder symptoms (DIrecT study)
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A 52‐week multicenter randomized controlled study of the efficacy and safety of add‐on dutasteride and imidafenacin to tamsulosin in patients with benign prostatic hyperplasia with remaining overactive bladder symptoms (DIrecT study)

机译:一项为期52周的多中心随机对照研究研究了度他雄胺和伊达非那星联合坦索罗辛治疗良性前列腺增生并伴有膀胱过度活动症的疗效和安全性(DIrecT研究)

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摘要

The aim of this study was to examine the long‐term efficacy of combination of tamsulosin 0.2 mg + dutasteride 0.5 mg + imidafenacin 0.2 mg (TDI) therapy compared with tamsulosin + dutasteride (TD) therapy for 52 weeks in benign prostatic hyperplasia (BPH) patients with a prostate volume (PV) ≥30 mL and remaining overactive bladder (OAB) symptoms after having received tamsulosin for ≥8 weeks. Previously, we reported that the improvement in OAB symptoms at 24 weeks was significantly greater in the TDI than TD group.
机译:这项研究的目的是检验坦索罗辛0.2 mg +达他雄胺0.5 mg +咪达芬那星0.2 mg(TDI)与坦索罗辛+达他雄胺(TD)疗法在良性前列腺增生(BPH)52周中的长期疗效接受坦索罗辛≥8周后,前列腺体积(PV)≥30mL且仍保留膀胱过度活动症(OAB)症状的患者。以前,我们报道TDI组在24周时OAB症状的改善明显大于TD组。

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