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首页> 外文期刊>Urologia internationalis >Non-Antibiotic Herbal Therapy (BNO 1045) versus Antibiotic Therapy (Fosfomycin Trometamol) for the Treatment of Acute Lower Uncomplicated Urinary Tract Infections in Women: A Double-Blind, Parallel-Group, Randomized, Multicentre, Non-Inferiority Phase III Trial
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Non-Antibiotic Herbal Therapy (BNO 1045) versus Antibiotic Therapy (Fosfomycin Trometamol) for the Treatment of Acute Lower Uncomplicated Urinary Tract Infections in Women: A Double-Blind, Parallel-Group, Randomized, Multicentre, Non-Inferiority Phase III Trial

机译:非抗生素草药治疗(BNO 1045)与抗生素治疗(FOSFOMYCIN TROFORAMOL)治疗急性较低的女性急性尿路感染:双盲,平行组,随机,多期,非劣级阶段III试验

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Introduction: This randomized, controlled, Phase III non-inferiority clinical trial aimed to determine whether herbal therapy with Canephron (R) N (BNO 1045) is non-inferior to fosfomycin trometamol (FT) in treating acute lower uncomplicated urinary tract infections (uUTIs). Materials and Methods: Women aged 18-70 years with typical symptoms of newly diagnosed acute lower uUTIs were randomized to BNO 1045 (n = 325) or FT (n = 334), with corresponding matched placebo. The primary endpoint was the proportion of patients who received additional antibiotics (ABs) to treat uUTIs between Days 1 and 38 +/- 3. Results: Between Days 1 and 38, 238 (83.5%) patients in the BNO 1045 group and 272 (89.8%) patients in the FT group received no additional ABs. At a 15% non-inferiority margin, BNO 1045 was non-inferior to FT in treating uUTIs (non-AB rate difference: -6.26%; 95% CI -11.99 to -0.53%; 2-sided p = 0.0014). Adverse event rates were similar between groups, with higher rates of gastrointestinal disorders in the FT group and pyelonephritis in the BNO 1045 group. During the trial, no patient died or discontinued due to a treatment-related adverse event. Conclusions: BNO 1045 has the potential to reduce outpatient use of ABs for uUTIs and thus may have a significant impact on antimicrobial stewardship strategies. Trial registration: NCT02639520, EudraCT number 2013-004529-99.
机译:介绍:这种随机,受控,第III期非劣级临床试验旨在确定与大脑(R)N(BNO 1045)的草药治疗是否是非较差的,在治疗急性低的简单尿路感染(Uutis )。材料和方法:18-70岁的女性随着新诊断的急性下部UUTIS的典型症状被随机化为BNO 1045(n = 325)或FT(n = 334),相应的匹配安慰剂。主要终点是接受额外抗生素(ABS)以治疗uutis的患者的比例,以在第1天和38 +/- 3之间治疗Uutis 89.8%)FT组的患者没有额外的ABS。在15%的非劣率余量下,BNO 1045在治疗UUTIS中非差(非AB速率差:-6.26%; 95%CI -11.99至-0.53%;双面P = 0.0014)。群体之间的不良事件率在FT组和BNO 1045组中具有较高的胃肠道疾病患者。在审判期间,由于治疗相关的不良事件,没有患者死亡或停止。结论:BNO 1045有可能减少对Uutis的ABS的门诊使用,因此可能对抗微生物管道战略产生重大影响。试验注册:NCT02639520,Eudract 2013-004529-99。

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