P E Van Kerrebroeck1. 1. Department of Urology in the University Hospital of Maastricht, Maastricht, The Netherlands. Pvk@suro.azm.nl
Abstract
OBJECTIVES: To assess the long-term efficacy and safety of alfuzosin 10 mg OD in patients with symptomatic BPH. METHODS:Patients (>50 years) were randomised to alfuzosin 10 mg OD, alfuzosin 2.5. mg t.i.d. or placebo for 3 months. Open-label alfuzosin 10 mg OD was continued for up to 1 year. Efficacy assessments included the International Prostate Symptom Score (I-PSS) and quality of life index and uroflowmetry. RESULTS: At 3 months, there was a significant reduction in I-PSS and a significant improvement in peak flow rate for both alfuzosin groups compared with placebo (p < 0.05). Vasodilatory adverse experiences were more common in the alfuzosin 2.5 mg group than the 10 mg OD group. Improvements in symptoms and flow rate with alfuzosin 10 mg OD were maintained for up to 12 months. CONCLUSION:Alfuzosin 10 mg OD is an effective treatment for symptomatic BPH for at least 12 months, with a better cardiovascular safety profile than the immediate release formulation.
RCT Entities:
OBJECTIVES: To assess the long-term efficacy and safety of alfuzosin 10 mg OD in patients with symptomatic BPH. METHODS:Patients (>50 years) were randomised to alfuzosin 10 mg OD, alfuzosin 2.5. mg t.i.d. or placebo for 3 months. Open-label alfuzosin 10 mg OD was continued for up to 1 year. Efficacy assessments included the International Prostate Symptom Score (I-PSS) and quality of life index and uroflowmetry. RESULTS: At 3 months, there was a significant reduction in I-PSS and a significant improvement in peak flow rate for both alfuzosin groups compared with placebo (p < 0.05). Vasodilatory adverse experiences were more common in the alfuzosin 2.5 mg group than the 10 mg OD group. Improvements in symptoms and flow rate with alfuzosin 10 mg OD were maintained for up to 12 months. CONCLUSION:Alfuzosin 10 mg OD is an effective treatment for symptomatic BPH for at least 12 months, with a better cardiovascular safety profile than the immediate release formulation.
Authors: Cosimo De Nunzio; Giorgio Franco; Costantino Leonardo; Alberto Trucchi; Andrea Tubaro; Cesare Laurenti Journal: Clin Drug Investig Date: 2005 Impact factor: 2.859