Low dose of cyproterone acetate and testosterone enanthate for contraception in men

dc.contributor.authorDi Cintio, Giulioen_US
dc.contributor.authorCostantino, Antoniettaen_US
dc.contributor.authorFlamigni, Carloen_US
dc.contributor.authorMeriggiola, M. Cristinaen_US
dc.contributor.authorBremner, William J.en_US
dc.date.accessioned2008-10-17T20:41:29Z
dc.date.available2008-10-17T20:41:29Z
dc.date.issued1998-05en_US
dc.description.abstractAfter a control phase, 10 normal men received cyproterone acetate (CPA) at a dose of 25 mg/day (CPA-25; n=5) or 12.5 mg/day (CPA-12.5; n=5) plus testosterone enanthate (TE) 100 mg/week, for 16 weeks. Throughout the study sperm counts were performed every 2 weeks, and luteinizing hormone (LH), follicle stimulating hormone (FSH), testosterone, biochemical and haematological tests were performed every 4 weeks. All five men in group CPA-25 and three men in group CPA-12.5 achieved azoospermia. One man in group CPA-25 was azoospermic by week 12 of hormone administration, but had a sperm count of 0.1 x 10(6)/ml at week 16. Time to azoospermia was 9.0+/-1.3 and 8.7+/-0.7 weeks in groups CPA-25 and CPA-12.5 respectively. Gonadotrophins were decreased by week 4 of hormone administration, remained around the minimum detectability of the assay for the duration of hormone administration and returned to baseline after stopping hormone administration. Testosterone values did not change. No change in any biochemical parameters was found. Haematological parameters were decreased at week 16 of hormone administration and returned to baseline after stopping hormone administration. In conclusion, these results suggest that an hormonal regimen consisting of testosterone plus a progestin with anti-androgenic properties holds promise as an effective, safe and reversible male contraceptive.en_US
dc.identifier.citationHum Reprod. 1998 May;13(5):1225-9en_US
dc.identifier.urihttp://hdl.handle.net/1773/4358
dc.language.isoen_USen_US
dc.publisherOxford University Pressen_US
dc.subjectmale contraceptionen_US
dc.subjectandrologyen_US
dc.subjectgonadotropinsen_US
dc.subject5-alpha reductase inhibitorsen_US
dc.subjectspermatogenesisen_US
dc.subjecttestosteroneen_US
dc.subjectcolchicineen_US
dc.subjectklinefelter's syndromeen_US
dc.subjectreifenstein's syndromeen_US
dc.subject.meshFollicle Stimulating Hormone, blooden_US
dc.subject.meshTestosterone, administration & dosage, adverse effects, analogs & derivatives, blooden_US
dc.subject.meshTime Factorsen_US
dc.subject.meshCyproterone Acetate, administration & dosage, adverse effectsen_US
dc.subject.meshHemoglobins, metabolismen_US
dc.subject.meshLipids, blooden_US
dc.subject.meshHematocriten_US
dc.subject.meshResearch Support, Non-U.S. Gov'ten_US
dc.subject.meshLuteinizing Hormone, blooden_US
dc.subject.meshMaleen_US
dc.subject.meshSperm Counten_US
dc.subject.meshHumansen_US
dc.subject.meshAdulten_US
dc.subject.meshContraceptive Agents, Male, administration & dosage, adverse effectsen_US
dc.subject.meshOligospermia, chemically induceden_US
dc.subject.meshTestis, drug effects, pathologyen_US
dc.subject.meshSpermatogenesis, drug effectsen_US
dc.subject.meshSafetyen_US
dc.titleLow dose of cyproterone acetate and testosterone enanthate for contraception in menen_US
dc.typeArticleen_US

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