Alfuzosin in the treatment of benign prostatic hyperplasia: effects on symptom scores, urinary flow rates and residual volume. A multicentre, double-blind, placebo-controlled trial. ALFECH Study Group.

Author(s): Hansen BJ, Nordling J, Mensink HJ, Walter S, Meyhoff HH

Affiliation(s): Department of Urology, Bispebjerg Hospital, Copenhagen, Denmark.

Publication date & source: 1994, Scand J Urol Nephrol Suppl., 157:169-76.

Publication type: Clinical Trial; Multicenter Study; Randomized Controlled Trial

In order to assess the efficacy and safety of alfuzosin, a selective alpha-1 receptor antagonist, 205 patients with Benign Prostatic Hyperplasia (BPH) were randomly assigned in a double-blind, placebo-controlled manner, to receive either alfuzosin 2.5 mg TID or placebo TID during 12 weeks. After 12 weeks symptom scores-assessed according to the Madsen-Iversen scale were significantly reduced in the alfuzosin group and peak flow rate significantly increased compared to the placebo group. There were no significant differences concerning adverse events or withdrawals. Alfuzosin proved to have a beneficial effect in patients with symptomatic BPH with few and minor adverse events.