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Study identifier: NCT07715448 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

Effect of Different Dosing Regimens of Tadalafil or Tamsulosin Combined With 5α-Reductase Inhibitors on Urinary and Sexual Outcomes in Benign Prostatic Hyperplasia

Condition: Benign Prostatic Hyperplasia · Lower Urinary Tract Symptoms · Erectile Dysfunction  ·  Sponsor: Beni-Suef University

PhasePhase 4
Planned participants240
Who can joinMale, 50 Years to no upper limit
Healthy volunteersNo

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About this study

Benign prostatic hyperplasia (BPH) is a common condition among aging men that causes lower urinary tract symptoms (LUTS) and may negatively affect sexual function. This randomized single-blind controlled clinical trial compares the efficacy, safety, and sexual outcomes of different dosing regimens of tadalafil or tamsulosin combined with 5-alpha reductase inhibitors (5ARIs) in men with BPH and enlarged prostate volume. A total of 240 participants were randomly assigned to six treatment groups and followed for 12 weeks. Changes in urinary symptoms, erectile function, ejaculatory function, prostate volume, prostate-specific antigen (PSA), urinary flow rate, post-void residual volume, and adverse events were evaluated to determine the optimal combination regimen.

This description comes directly from the study's public registry record.

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Locations (1)

Beni-Suef University HospitalBanī Suwayf, Beni Suef Governorate, Egypt

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