Comparison of alpha blockers in treatment of premature ejaculation: A pilot clinical trial

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Özet

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. © 2013, Kowsar. All Rights Reserved.

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https://rdlopen.rawdatalibrary.net/r/ebyu/15765Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.5812/ircmj.13805Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorAkin, Yigit
dc.contributor.authorGulmez, Hakan
dc.contributor.authorAtes, Mutlu
dc.contributor.authorBozkurt, Aliseydi
dc.contributor.authorNuhoglu, Baris
dc.date.accessioned2026-10-18T20:30:36.622750301Z
dc.date.available2026-10-18T20:30:36.622750301Z
dc.date.issued2013
dc.description.abstractBackground: 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. © 2013, Kowsar. All Rights Reserved.
dc.identifier.doi10.5812/ircmj.13805
dc.identifier.issn2074-1804
dc.identifier.issue10
dc.identifier.scopus2-s2.0-84887283014
dc.identifier.startpagee13805
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15765
dc.identifier.volume15
dc.language.isoen
dc.publisherIranian Red Crescent Society
dc.relation.ispartofIranian Red Crescent Medical Journal
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPremature ejaculation
dc.subjectQuality of life
dc.subjectSerotonin uptake inhibitors
dc.subjectalfuzosin
dc.subjectalpha adrenergic receptor blocking agent
dc.subjectdoxazosin mesylate
dc.subjectprostate specific antigen
dc.subjectsilodosin
dc.subjecttamsulosin
dc.subjectterazosin
dc.subjectadult
dc.subjectaged
dc.subjectarticle
dc.subjectchronic prostatitis
dc.subjectdizziness
dc.subjectdrug abuse
dc.subjectdrug efficacy
dc.subjectdrug safety
dc.subjectejaculation disorder
dc.subjectfollow up
dc.subjecthomosexuality
dc.subjecthuman
dc.subjectintravaginal ejaculation latency time
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectorthostatic hypotension
dc.subjectpilot study
dc.subjectPremature Ejaculation Profile
dc.subjectrandomized controlled trial
dc.subjecttreatment outcome
dc.titleComparison of alpha blockers in treatment of premature ejaculation: A pilot clinical trial
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus27
rdl.oa.statusgreen
rdl.source.indexSCOPUS