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Comparing monotherapy with tadalafil or tamsulosin in men with benign prostatic hyperplasia: A case-control study

Hayder Adnan Fawzi, Saif Akram, A. Talib, Mustafa Hasan Alwan, L. A. Yasir

Journal of Advanced Pharmaceutical Technology & Research, 2024

100 participants · 2 citations

Abstract

Benign prostatic hyperplasia (BPH) is a chronic disorder that inflicts severe symptoms on middle-aged men. The current study compared the effects of tadalafil and tamsulosin on urological parameters after 3 and 6 months of therapy. A retrospective case–control study was conducted, in which 100 patients with moderately severe BPH were divided into two groups based on their treatment: 50 patients were given tamsulosin 0.4 mg/day and group 50 patients were administered tadalafil 5 mg daily. All patients continued therapy for approximately 6 months, and their urological parameters were assessed at baseline and after 3 and 6 months. There was no significant difference in the overall effect on the International Prostate Symptom Score at the end of the study using two-way ANOVA analysis ( P = 0.448). The intercourse number was significantly improved by tadalafil compared to tamsulosin ( P < 0.001). The prostatic-specific antigen, postvoiding residual, and prostatic volumes were not significantly different between tadalafil and tamsulosin ( P = 0.198, 0.163, and 0.183, respectively). In conclusion, tadalafil, 5 mg once daily, appears to have similar efficacy to tamsulosin, with significant improvement in the patient’s erectile function. Tadalafil can be used for 6 months for moderate-to-severe lower urinary tract symptoms.

How strong is the evidence?

Evidence Hub reads this as a case-control, done in people. Its evidence level is 4 of 5 (Low · observational). Observational designs can show an association but not prove cause. Reported size: 100 participants or records.

How the five levels of evidence work. The level is assigned automatically from the abstract and can be wrong, so check the paper.

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