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Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial

BACKGROUND: Premature ejaculation (PE) is the most common sexual disorder in men and studies reported prevalence up to 30% (1, 2). PE is not a life-threatening medical condition but it influences the quality of life (QoL). OBJECTIVES: The aim of this study was to compare the efficiency, and safety o...

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Autores principales: Akin, Yigit, Gulmez, Hakan, Ates, Mutlu, Bozkurt, Aliseydi, Nuhoglu, Baris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950775/
https://www.ncbi.nlm.nih.gov/pubmed/24693363
http://dx.doi.org/10.5812/ircmj.13805
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author Akin, Yigit
Gulmez, Hakan
Ates, Mutlu
Bozkurt, Aliseydi
Nuhoglu, Baris
author_facet Akin, Yigit
Gulmez, Hakan
Ates, Mutlu
Bozkurt, Aliseydi
Nuhoglu, Baris
author_sort Akin, Yigit
collection PubMed
description BACKGROUND: Premature ejaculation (PE) is the most common sexual disorder in men and studies reported prevalence up to 30% (1, 2). PE is not a life-threatening medical condition but it influences the quality of life (QoL). OBJECTIVES: The aim of this study was to compare the efficiency, and safety of alpha blocker drugs in the treatment of patients with premature ejaculation (PE). Additionally we investigated the quality of life (QoL) in patients with PE who were treated with alpha blocker drugs. MATERIALS AND METHODS: This study was a pilot clinical trial. Prospectively documented 108 patients with PE were treated and were followed-up in urology outpatient clinic. All patients were divided into 5 groups according to used alpha blocker agents which were determined by simple randomization. Silodosin 4mg (Group 1, n = 21), tamsulosin hydrochloride 0.4mg (Group 2, n = 23), alfuzosin 10mg (Group 3, n = 22), terazosin 5mg (Group 4, n = 21), doksazosin mesylate 4mg (Group5, n = 21), were used for treatment. The demographic parameters of patients, pre and post treatment intravaginal ejaculation latency time (IELT), PE Profile (PEP), and QoL index were recorded and evaluated. Effectiveness of treatment was evaluated by measuring IELT. Additionally, side effects of drugs were recorded. P < 0.05 was considered statistically significant. RESULTS: All alpha blocker drugs were statistically effective for preventing PE. Notably, silodosin seemed to be more effective for preventing PE than other alpha blockers (P < 0.05). However all alpha blockers provided development in QoL scores, silodosin was a little better than other drugs in statistical analyses. Furthermore statistical increase in IELT and decrease in PEP were provided more in Group 1 than other groups (P < 0.05). CONCLUSIONS: Silodosin seems to be able to even more prevent PE. Silodosin may provide development in QoL than other alpha blocker agents. Additionally, lower systemic adverse events and more effectivity are the prominent features of silodosin in PE.This study was a pilot clinical trial. Prospectively documented 108 patients with PE were treated and were followed-up in urology outpatient clinic. All patients were divided into 5 groups according to used alpha blocker agents which were determined by simple randomization. Silodosin 4mg (Group 1, n = 21), tamsulosin hydrochloride 0.4mg (Group 2, n = 23), alfuzosin 10mg (Group 3, n = 22), terazosin 5mg (Group 4, n = 21), doksazosin mesylate 4mg (Group5, n = 21), were used for treatment. The demographic parameters of patients, pre and post treatment intravaginal ejaculation latency time (IELT), PE Profile (PEP), and QoL index were recorded and evaluated. Effectiveness of treatment was evaluated by measuring IELT. Additionally, side effects of drugs were recorded. P < 0.05 was considered statistically significant.
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spelling pubmed-39507752014-04-01 Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial Akin, Yigit Gulmez, Hakan Ates, Mutlu Bozkurt, Aliseydi Nuhoglu, Baris Iran Red Crescent Med J Research Article BACKGROUND: Premature ejaculation (PE) is the most common sexual disorder in men and studies reported prevalence up to 30% (1, 2). PE is not a life-threatening medical condition but it influences the quality of life (QoL). OBJECTIVES: The aim of this study was to compare the efficiency, and safety of alpha blocker drugs in the treatment of patients with premature ejaculation (PE). Additionally we investigated the quality of life (QoL) in patients with PE who were treated with alpha blocker drugs. MATERIALS AND METHODS: This study was a pilot clinical trial. Prospectively documented 108 patients with PE were treated and were followed-up in urology outpatient clinic. All patients were divided into 5 groups according to used alpha blocker agents which were determined by simple randomization. Silodosin 4mg (Group 1, n = 21), tamsulosin hydrochloride 0.4mg (Group 2, n = 23), alfuzosin 10mg (Group 3, n = 22), terazosin 5mg (Group 4, n = 21), doksazosin mesylate 4mg (Group5, n = 21), were used for treatment. The demographic parameters of patients, pre and post treatment intravaginal ejaculation latency time (IELT), PE Profile (PEP), and QoL index were recorded and evaluated. Effectiveness of treatment was evaluated by measuring IELT. Additionally, side effects of drugs were recorded. P < 0.05 was considered statistically significant. RESULTS: All alpha blocker drugs were statistically effective for preventing PE. Notably, silodosin seemed to be more effective for preventing PE than other alpha blockers (P < 0.05). However all alpha blockers provided development in QoL scores, silodosin was a little better than other drugs in statistical analyses. Furthermore statistical increase in IELT and decrease in PEP were provided more in Group 1 than other groups (P < 0.05). CONCLUSIONS: Silodosin seems to be able to even more prevent PE. Silodosin may provide development in QoL than other alpha blocker agents. Additionally, lower systemic adverse events and more effectivity are the prominent features of silodosin in PE.This study was a pilot clinical trial. Prospectively documented 108 patients with PE were treated and were followed-up in urology outpatient clinic. All patients were divided into 5 groups according to used alpha blocker agents which were determined by simple randomization. Silodosin 4mg (Group 1, n = 21), tamsulosin hydrochloride 0.4mg (Group 2, n = 23), alfuzosin 10mg (Group 3, n = 22), terazosin 5mg (Group 4, n = 21), doksazosin mesylate 4mg (Group5, n = 21), were used for treatment. The demographic parameters of patients, pre and post treatment intravaginal ejaculation latency time (IELT), PE Profile (PEP), and QoL index were recorded and evaluated. Effectiveness of treatment was evaluated by measuring IELT. Additionally, side effects of drugs were recorded. P < 0.05 was considered statistically significant. Kowsar 2013-10-05 2013-10 /pmc/articles/PMC3950775/ /pubmed/24693363 http://dx.doi.org/10.5812/ircmj.13805 Text en Copyright © 2013, Iranian Red Crescent Medical Journal; Licensee Kowsar Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Akin, Yigit
Gulmez, Hakan
Ates, Mutlu
Bozkurt, Aliseydi
Nuhoglu, Baris
Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial
title Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial
title_full Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial
title_fullStr Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial
title_full_unstemmed Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial
title_short Comparison of Alpha Blockers in Treatment of Premature Ejaculation: A Pilot Clinical Trial
title_sort comparison of alpha blockers in treatment of premature ejaculation: a pilot clinical trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950775/
https://www.ncbi.nlm.nih.gov/pubmed/24693363
http://dx.doi.org/10.5812/ircmj.13805
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