Efficacy and Safety of Once Daily Administration Tadalafil in Patients With Benign Prostatic Hyperplasia
Abstract
The aim of the present study is to evaluate the efficacy and safety of once daily administration PDE5 inhibitors, tadalafil for 3 months as anti-inflammatory, antiproliferative and relaxant effects in ED with BPH patients.
Conditions: BPH With Other Lower Urinary Tract Symptoms.
Primary outcome: Evaluation of International prostate symptom score (IPSS)/quality of life (QoL).; Evaluation of International index of erectile function (IIEF)..
Enrollment: 306 participants.
How strong is the evidence?
Evidence Hub reads this as a clinical trial, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 306 participants or records.
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