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癃闭舒胶囊联合多沙唑嗪治疗良性前列腺增生症的疗效:一项随机对照试验。

Effect of Longbishu capsule () plus doxazosin on benign prostatic hyperplasia: a randomized controlled trial.

作者信息

Song Chun-Sheng, Guo Jun, Chang De-Gui, Chen Lei, Zhang Rui, Zhao Jia-You, Wang Fu, Zhang Qiang

机构信息

Graduate School of China Academy of Chinese Medical Sciences, Beijing, 100700, China,

出版信息

Chin J Integr Med. 2014 Nov;20(11):818-22. doi: 10.1007/s11655-014-1844-0. Epub 2014 Jun 18.

Abstract

OBJECTIVE

To investigate the effect of Longbishu Capsule (, LBS), doxazosin, and combination therapy on benign prostatic hyperplasia (BPH).

METHODS

A randomized, double-blind, multi-center parallel trial was conducted involving 360 patients in hospitals in Beijing (108 cases), Heilongjiang (90 cases), Sichuan (90 cases), Shanghai (72 cases), China. They were randomly assigned with central randomization method to group A (LBS placebo plus doxazosin), group B (LBS plus doxazosin) or group C (LBS plus doxazosin placebo), 120 cases for each group. The international prostate symptom score, maximum urinary flow rate, postvoid residual urine volume and prostate volume were measured for evaluating the efficacy of the three treatments.

RESULTS

At baseline, there was no significant difference in the measured variables among the three groups. After 12-month treatment, the three groups showed significant improvements in IPSS and maximum urinary flow rate from baseline (P<0.01). Although postvoid residual urine volume was not significantly different from the baseline in group A (P>0.05), it significantly decreased in group B and C (P<0.05). The incidence of adverse events were similar among the three groups.

CONCLUSIONS

The treatment of LBS alone or LBS plus doxazosin was able to significantly improve IPSS in patients with BPH. The treatments may reduce the increase in prostate volume and postvoid residual urine volume as well.

摘要

目的

探讨龙必舒胶囊(LBS)、多沙唑嗪及联合治疗对良性前列腺增生(BPH)的影响。

方法

进行一项随机、双盲、多中心平行试验,纳入中国北京(108例)、黑龙江(90例)、四川(90例)、上海(72例)等地医院的360例患者。采用中心随机化方法将他们随机分为A组(LBS安慰剂加多沙唑嗪)、B组(LBS加多沙唑嗪)或C组(LBS加多沙唑嗪安慰剂),每组120例。测量国际前列腺症状评分、最大尿流率、排尿后残余尿量和前列腺体积,以评估三种治疗方法的疗效。

结果

基线时,三组间测量变量无显著差异。治疗12个月后,三组的国际前列腺症状评分和最大尿流率较基线均有显著改善(P<0.01)。虽然A组排尿后残余尿量与基线无显著差异(P>0.05),但B组和C组显著降低(P<0.05)。三组不良事件发生率相似。

结论

单独使用LBS或LBS加多沙唑嗪治疗能够显著改善BPH患者的国际前列腺症状评分。这些治疗方法还可能减少前列腺体积增加和排尿后残余尿量。

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