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. 2015 Oct;7(5):249–264. doi: 10.1177/1756287215589238

Table 2.

Mean changes from baseline to end point in total IPSS, IPSS subscores, IPSS quality of life index, and maximum flow rate in 12-week, double-blind, randomized, placebo-controlled clinical studies of tamsulosin in men with lower urinary tract symptoms secondary to benign prostatic hyperplasia.

Study Treatment n Mean change from baseline
Total IPSS IPSS storage subscore IPSS voiding subscore IPSS QoL index Qmax, ml/s
Asian studies$
Yokoyama et al. [2013] Placebo 154 −3.0 −1.1 −1.9 −0.5 2.1
Tadalafil 5 mg 155 −4.7* −1.7* −3.0* −0.8* 1.3
Tamsulosin 0.2 mg 152 −5.5 −1.7 −3.8 −1.1 2.1
Kawabe et al. [2006] Placebo 89 −5.3 −1.5 −3.8 −1.1 0.3
Tamsulosin 0.2 mg 192 −6.8 −2.1 −4.8 −1.4 2.6
Kim et al. [2011] Placebo 51 −4.2 −1.5 −2.7 −0.9 2.3
Tadalafil 5 mg 51 −5.8 −2.1 −3.7 −1.2 2.5
Tamsulosin 0.2 mg 49 −5.4 −1.8 −3.6 −1.0 2.1
Non-Asian study
Oelke et al. [2012] Placebo 172 −4.2 −1.6 −2.6 −1.0 1.2
Tadalafil 5 mg 171 −6.3* −2.2 −4.1* −1.3* 2.4*
Tamsulosin 0.4 mg 168 −5.7* −2.2 −3.5* −1.1 2.2*
*

p < 0.05 versus placebo.

$

Tamsulosin versus placebo statistical comparisons were not made in the studies reported by Kawabe et al. [2006] and Yokoyama et al. [2013].

IPSS, International Prostate Symptom Score; n, number of randomized participants; Qmax, maximum urinary flow rate; QoL, quality of life.