Actively Recruiting

Phase 3
Age: 40Years - 70Years
MALE
NCT06491108

Medications for Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia

Led by Tanta University · Updated on 2024-07-08

150

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of this prospective randomized controlled study is to compare safety and efficacy of Vardenafil versus Tadalafil versus Tamsulosin in terms of (voiding function, sexual function and quality of life) in the management of moderate BPH related LUTS.

CONDITIONS

Official Title

Medications for Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia

Who Can Participate

Age: 40Years - 70Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Sexually active men
  • Moderate benign prostatic hyperplasia related lower urinary tract symptoms with an International Prostate Symptom Score between 8 and 19
  • Patients who accepted medical treatment and completed 12 weeks of treatment with strict follow-up
Not Eligible

You will not qualify if you...

  • Need for combined therapy due to prostate size over 40 grams
  • Presence of gross hematuria
  • Refractory urinary retention
  • Bilateral hydro-ureteronephrosis or kidney problems caused by benign prostatic hyperplasia
  • Bladder diverticula or bladder stones
  • History of bladder or prostate cancer
  • Unwillingness to receive medical therapy
  • History of pelvic surgery or urethral stricture

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculity of medicine - Tanta university

Tanta, Gharbia Governorate, Egypt, 31528

Actively Recruiting

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Research Team

H

Hazem B. Baz, M.B.B.Ch

CONTACT

M

Mohamed G. Soliman, M.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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