ORIGINAL PAPER A randomised, double-blind study comparing the efficacy and tolerability of controlled-release doxazosin and tamsulosin in the treatment of benign prostatic hyperplasia in Brazil

• Published in: International journal of clinical practice (Esher) Vol. 60; no. 10; pp. 1172 - 1177
• Main Authors: Pompeo, ACL, Rosenblatt, C, Bertero, E, DA Ros, CT, Cairoli, CED, Damiao, R, Wroclawski, E R, Koff, W J, Mesquita, F, Pinheiro, GE
• Format: Journal Article
• Language: English
• Published: London Hindawi Limited 01.10.2006
• Subjects: Clinical outcomes; Disease; Drug therapy; Prostate; Brazil
• ISSN: 1368-5031; 1742-1241
• DOI: 10.1111/j.1742-1241.2006.01107.x

Brazilian patients with benign prostatic hyperplasia were randomised in a 12-week, double-blind, double-dummy study to receive doxazosin gastrointestinal therapeutic system (GITS) 4 mg q.i.d. (n = 82) or tamsulosin 0.4 q.i.d. (n = 83). Primary endpoints were the absolute and percentage change from baseline in symptoms measured by International Prostate Symptom Score (IPSS). Secondary endpoints included IPSS, quality-of-life (QOL) question from the IPSS, and questions 6 and 7 of the Sexual Function Abbreviated Questionnaire (SFAQ) at weeks 4 and 12. Doxazosin GITS and tamsulosin improved IPSS with no significant differences between groups at week 12. During weeks 4-8, tamsulosin-treated patients demonstrated a slower improvement (p < 0.001) in IPSS than doxazosin GITS-treated patients. The proportion of satisfied patients was observed earlier with doxazosin GITS (p = 0.006) vs. tamsulosin. At week 12, the proportion of patients with little or no difficulty at ejaculation (Q6 of SFAQ) was higher in the doxazosin GITS group (p = 0.019). Both treatments were well tolerated.