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首页> 外文期刊>BMC Urology >Silodosin 8?mg improves benign prostatic obstruction in Caucasian patients with lower urinary tract symptoms suggestive of benign prostatic enlargement: results from an explorative clinical study
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Silodosin 8?mg improves benign prostatic obstruction in Caucasian patients with lower urinary tract symptoms suggestive of benign prostatic enlargement: results from an explorative clinical study

机译:Silodosin 8?MG在高加索患者中提高了尿路症状的高加索患者良性前列腺梗阻暗示良性前列腺肿大:探索性临床研究的结果

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To preliminary investigate the effects of silodosin 8?mg once daily on obstruction urodynamic parameters and subjective symptoms in Caucasian patients with lower urinary tract symptoms suggestive of benign prostatic enlargement. We performed a single-center, open-label, single-arm, post-marketing interventional clinical trial. Inclusion criteria were: Caucasian subjects aged ≥50?years waiting to undergo surgery for lower urinary tract symptoms suggestive of benign prostatic enlargement, international prostate symptom total score ≥ 13, international prostate symptom-quality of life score?≥?3, prostate volume ≥ 30?ml, maximum urine flow rate?≤?15?mL/s, bladder outlet obstruction index >?40. Eligible subjects received one capsule of silodosin 8?mg once daily for 8?weeks. Invasive urodynamic evaluations were performed at baseline and at 8-weeks follow-up. International prostate symptom questionnaire was administered at baseline, after 4-weeks and 8-weeks of treatment. Overall, 34 subjects were included. Mean bladder outlet obstruction index significantly decreased from 70.6 to 39.2 and bladder outlet obstruction index class improved in 16 patients (53.3%). Statistically significant improvements of mean total international prostate symptom score, mean storage sub-score, mean voiding sub-score and mean quality of life sub-score were evident after 4-weeks of treatment with further improvements after 8-weeks. At the end of the treatment, all patients declared that their condition improved enough to spare or delay surgery. Silodosin 8?mg once daily significantly improves benign prostatic obstruction in Caucasian patients with lower urinary tract symptoms suggestive of benign prostatic enlargement waiting for surgery. EudraCT n. 2015-002277-38 Date of registration: 15th December 2017.
机译:初步探讨每天硅二蛋白酶8?MG的影响,在患有尿路症状的白种人患者中的梗阻尿动力学参数和主观症状暗示良性前列腺肿大。我们进行了单一中心,开放标签,单臂,营销后介入临床试验。纳入标准是:白种人受试者年龄≥50岁,等待接受手术的尿路症状良好的前列腺肿大,国际前列腺症状总分≥13,国际前列腺症状 - 生活质量得分≥?3,前列腺素≥ 30?ml,最大尿液流速?≤α15?ml / s,膀胱出口障碍指数> 40。符合条件的受试者每天收到一次硅霉素8?MG的胶囊8?周。侵入性尿动力学评估在基线和8周后进行。国际前列腺症状调查问卷在基线,4周和8周治疗后给药。总体而言,包括34个科目。平均膀胱出口障碍指数从70.6到39.2显着降低,16名患者(53.3%)改善了膀胱出口障碍指数阶级。平均国际前列腺症状评分的统计学显着改善,平均储存分数,平均空隙分量和平均生活质量在4周后在8周后进一步改善后显而易见的。在治疗结束时,所有患者宣布其病症足以备用或延迟手术。硅霉素8?MG每日一次,在高加索患者中显着改善尿路患者的良性前列腺梗阻暗示良性前列腺增大等待手术。 eudract n。 2015-002277-38日期(注册):2017年12月15日。

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