Abstract |
This study was designed to determine the efficacy of the 5 alpha-reductase inhibitor finasteride (Proscar, MK-906) in men with reduced urinary flow rates and symptoms of urinary outflow obstruction secondary to benign prostatic hyperplasia. Forty-five men were randomized to one of three groups receiving either placebo, 1 mg/day or 5 mg/day finasteride for the first 12 months of the study period. At the end of this period all men received 5 mg/day finasteride for a further 2 years. Efficacy was determined by measurement of prostate volume, maximum urinary flow rate, and symptom score using a modified Boyarsky assessment. Prostate volume reduced by 20 and 27%, respectively, for those on 1 and 5 mg after the first year. At 3 years the volume had reduced by 43%. This reduction in prostate volume was associated with an improvement in maximum urinary flow rate by 50% (1 mg), and 35% (5 mg) at 1 year, and 36% at 3 years. The total, obstructive and non-obstructive symptom scores decreased (improved) for patients on 1 and 5 mg finasteride, with the total score reducing by 33% from baseline at year 3. The results demonstrate that finasteride causes a modest but significant clinical improvement in men with urinary outflow obstruction secondary to benign prostatic hyperplasia.
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Authors | J N Nacey, P J Meffan, B Delahunt |
Journal | The Australian and New Zealand journal of surgery
(Aust N Z J Surg)
Vol. 65
Issue 1
Pg. 35-9
(Jan 1995)
ISSN: 0004-8682 [Print] Australia |
PMID | 7529489
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
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Topics |
- Aged
- Double-Blind Method
- Finasteride
(administration & dosage, pharmacology, therapeutic use)
- Humans
- Male
- Middle Aged
- Prostate
(drug effects, pathology)
- Prostatic Hyperplasia
(drug therapy, physiopathology)
- Urodynamics
(drug effects)
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