MedPath

A Prospective Randomized Controlled Trial Assessing the Efficacy of Withdrawing Alpha-blocker Following Initial Combination Therapy with 5-Alpha Reductase Inhibitor for Benign Prostatic Hyperplasia

Not Applicable
Completed
Conditions
Benign Prostate Hyperplasia
Renal and Urogenital - Other renal and urogenital disorders
Registration Number
ACTRN12612000853842
Lead Sponsor
niversiti Kebangsaan Malaysia Medical Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Male
Target Recruitment
102
Inclusion Criteria

patients with moderate or severe BPH based on IPSS score who were newly diagnosed and started on combination therapy or who were previously diagnosed and were already on combination therapy for a duration of not more than one year. All patients on combination therapy had a prostate size of more than 40g as assessed by digital rectal examination

Exclusion Criteria

All patients had a baseline PSA taken routinely and patients with a value higher than 4ng/ml underwent biopsy to screen for possible malignancy. Patients with PSA value less than 1.5ng/ml, prostate cancer and patients with recurrent urinary tract infections were excluded from our study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
International Prostate Symptoms Score[Basline and 3 months]
Secondary Outcome Measures
NameTimeMethod
Maximal urinary Flow Rate via uroflowmeter equipment[baseline and 3 months]
© Copyright 2025. All Rights Reserved by MedPath