PMID- 26169181 OWN - NLM STAT- MEDLINE DCOM- 20160223 LR - 20181202 IS - 1872-6976 (Electronic) IS - 0167-4943 (Linking) VI - 61 IP - 2 DP - 2015 Sep-Oct TI - A randomized, controlled trial of effectiveness and safety of management of OAB symptoms in elderly men and women with standard-dosed combination of solifenacin and mirabegron. PG - 212-6 LID - S0167-4943(15)30010-8 [pii] LID - 10.1016/j.archger.2015.06.006 [doi] AB - OBJECTIVES: Comparison of effectiveness and safety of solifenacin and mirabegron, as well as their combination, for managing heavy symptoms of overactive bladder. MATERIALS AND METHODS: All patients who participated in the examination (average age: 71.2) were split into 4 groups. Patients included in Group capital A, Cyrillic (n=63) were treated with mirabegron 50mg/day/6 weeks, in Group B (n=52)-with solifenacin 10mg/day/6 weeks, in Group capital ES, Cyrillic (n=65)-with the same doses of both drugs simultaneously/6 weeks, and in Group D (n=59)-with placebo. Monitoring was carried out using OAB-questionnaires, bladder diaries and urodynamic examination. RESULTS: In elderly patients with initial frequency of episodes of incontinence (EI)>/=3/day standard doses of mirabegron (50mg/day) and solifenacin 10mg/day administered during 6 weeks result with the decrease in frequency of EI with high correlation (r=0,74, p1.6 per day, p5.3 per day, p29.9, p