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TREATMENT OF PREMATURE EJACULATION WITH PAROXETINE HYDROCHLORIDE AS NEEDED: 2 SINGLE-BLIND PLACEBO CONTROLLED CROSSOVER STUDIES

帕罗西汀 早泄 安慰剂 医学 交叉研究 射精 麻醉 随机对照试验 泌尿科 内科学 心理学 抗抑郁药 替代医学 病理 海马体 精神分析
作者
Chris G. McMahon,Kamal Touma
出处
期刊:The Journal of Urology [Ovid Technologies (Wolters Kluwer)]
卷期号:161 (6): 1826-1830 被引量:144
标识
DOI:10.1016/s0022-5347(05)68816-7
摘要

No AccessJournal of UrologyClinical Urology: Original Articles1 Jun 1999TREATMENT OF PREMATURE EJACULATION WITH PAROXETINE HYDROCHLORIDE AS NEEDED: 2 SINGLE-BLIND PLACEBO CONTROLLED CROSSOVER STUDIES CHRIS G. McMAHON and KAMAL TOUMA CHRIS G. McMAHONCHRIS G. McMAHON and KAMAL TOUMAKAMAL TOUMA View All Author Informationhttps://doi.org/10.1016/S0022-5347(05)68816-7AboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: We evaluate the efficacy of paroxetine hydrochloride as needed for the treatment of premature ejaculation. Materials and Method: Study 1 comprised 26 potent men with a mean age of 39.5 years with premature ejaculation who were randomized to receive 20 mg. oral paroxetine (group A) or placebo (group B) as needed 3 to 4 hours before planned intercourse in a controlled single-blind crossover trial. Study 2 comprised 42 potent men with a mean age of 40.5 years with premature ejaculation who were randomized to receive 10 mg. paroxetine daily for 3 weeks and then 20 mg. paroxetine as needed (group C) for 4 weeks or placebo daily for 3 weeks and then placebo as needed (group D) for 4 weeks. Results: Mean pretreatment ejaculatory latency time was 0.3 minute for study 1. At 4 weeks mean ejaculatory latency time was 3.2 minutes in the paroxetine as needed and 0.45 in the placebo as needed phase for group A (p <0.001), and 0.6 in the placebo as needed and 3.5 in the paroxetine as needed phase for group B (p <0.001). There were no adverse effects with paroxetine or placebo in study 1. Mean pretreatment ejaculatory latency time was 0.5 minute for study 2. At 3 weeks mean ejaculatory latency time was 4.3 minutes in the paroxetine daily and 5.8 in the paroxetine as needed phase, and 0.9 in the placebo daily and 0.6 in the placebo as needed phase for group C (p <0.001). At 3 weeks mean ejaculatory latency time was 0.8 minutes in the placebo daily and 1.1 in the placebo as needed phase, and 3.3 in the paroxetine daily and 6.1 in the paroxetine as needed phase for group D (p <0.001). Adverse effects in 7 of 42 men (17%) given paroxetine daily included anejaculation in 3, anorexia in 1, gastrointestinal upset in 3 and reduced libido in 2. Mean ejaculatory latency time was greater in the paroxetine as needed phase of study 2 than that of study 1 (p <0.05). suggesting that ejaculatory control achieved with paroxetine as needed is significantly better if patients are initially treated with the drug daily. Conclusions: Paroxetine appears to be superior to placebo in the pharmacological treatment of premature ejaculation when administered on a chronic or as needed basis. References 1 . Washington, D. C.: American Psychiatric Association1994: 509. Google Scholar 2 : Brain monoaminergic control of male reproductive behaviour. II. 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Crossref, Medline, Google Scholar 16 : Ejaculation-retarding properties of paroxetine in men with primary premature ejaculation: a double-blind, randomized, dose-response study. Brit. J. Urol.1997; 79: 592. Google Scholar 17 : Paroxetine in the treatment of premature ejaculation. Brit. J. Urol.1996; 77: 881. Crossref, Medline, Google Scholar 18 : Paroxetine in the treatment of premature ejaculation. Arch. Ital. Urol. Androl.1997; 69: 11. Google Scholar 19 McMahon, C.G.: Treatment of premature ejaculation with paroxetine hydrochloride. Int. J. Impotence Res., suppl., 9: S38, abstract 36. Google Scholar 20 : Paroxetine: pharmacokinetics and pharmacodynamics. Fortschritte der Neurologie-Psychiatrie1994; 62: 2. Google Scholar 21 : The role of cytochrome P450 2D6 in the metabolism of paroxetine by human liver microsomes. Brit. J. Clin. Pharmacol.1992; 33: 531. Google Scholar 22 : Pharmacokinetics of anti-depressants: why and how they are relevant to treatment. J. Clin. Psychiat.1993; 54: 14. Google Scholar 23 : A review of the metabolism and pharmacokinetics of paroxetine in man. Acta Psychiat. Scand.1991; 80: 60. Google Scholar From St. Luke's Hospital Complex, Sydney, Australia© 1999 by American Urological Association, Inc.FiguresReferencesRelatedDetailsCited byShindel A, Althof S, Carrier S, Chou R, McMahon C, Mulhall J, Paduch D, Pastuszak A, Rowland D, Tapscott A and Sharlip I (2021) Disorders of Ejaculation: An AUA/SMSNA GuidelineJournal of Urology, VOL. 207, NO. 3, (504-512), Online publication date: 1-Mar-2022.Giuliano F, Bernabé J, Gengo P, Alexandre L and Clément P (2018) Effect of Acute Dapoxetine Administration on the Pudendal Motoneuron Reflex in Anesthetized Rats: Comparison With ParoxetineJournal of Urology, VOL. 177, NO. 1, (386-389), Online publication date: 1-Jan-2007.Motofei I (2018) RE: The Neurobiological Approach to Premature EjaculationJournal of Urology, VOL. 170, NO. 3, (929-929), Online publication date: 1-Sep-2003.SALONIA A, MAGA T, COLOMBO R, SCATTONI V, BRIGANTI A, CESTARI A, GUAZZONI G, RIGATTI P and MONTORSI F (2018) A Prospective Study Comparing Paroxetine Alone Versus Paroxetine Plus Sildenafil in Patients With Premature EjaculationJournal of Urology, VOL. 168, NO. 6, (2486-2489), Online publication date: 1-Dec-2002.WALDINGER M (2018) The Neurobiological Approach to Premature EjaculationJournal of Urology, VOL. 168, NO. 6, (2359-2367), Online publication date: 1-Dec-2002. Volume 161Issue 6June 1999Page: 1826-1830 Advertisement Copyright & Permissions© 1999 by American Urological Association, Inc.MetricsAuthor Information CHRIS G. McMAHON More articles by this author KAMAL TOUMA More articles by this author Expand All Advertisement PDF downloadLoading ...
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