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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/66130
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dc.contributor.authorGentil, Valentim-
dc.contributor.authorTiosso, Ana-
dc.contributor.authorBenedictis, Eliana-
dc.contributor.authorKerr-Correa, Florence-
dc.contributor.authorMoreno, Ricardo-
dc.contributor.authorD'Arrigo Busnello, Ellis-
dc.contributor.authorCampos, João Alberto de-
dc.contributor.authorJuruena, Mario Francisco-
dc.contributor.authorLafer, Beny-
dc.contributor.authorMoreno, Doris Hupfeld-
dc.contributor.authorRosa, Lucena de Cássia Rodrigues-
dc.date.accessioned2014-05-27T11:19:54Z-
dc.date.accessioned2016-10-25T18:16:20Z-
dc.date.available2014-05-27T11:19:54Z-
dc.date.available2016-10-25T18:16:20Z-
dc.date.issued2000-03-29-
dc.identifierhttp://dx.doi.org/10.1177/026988110001400108-
dc.identifier.citationJournal of Psychopharmacology, v. 14, n. 1, p. 61-66, 2000.-
dc.identifier.issn0269-8811-
dc.identifier.urihttp://hdl.handle.net/11449/66130-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/66130-
dc.description.abstractThe purpose of this study was to compare the efficacy and tolerability of venlafaxine and amitriptyline in outpatients with major depression with or without melancholia. This was an 8-week, multicentre, randomized, double-blind, parallel-group comparison of venlafaxine and amitriptyline. Outpatients with DSM-IV major depression, a minimum score of 20 on the 21-item Hamilton Depression Rating Scale (HAM-D), and depressive symptoms for at least 1 month were eligible. Patients were randomly assigned to venlafaxine or amitriptyline, both drugs titrated to a maximum of 150 mg/day until study day 15. The primary efficacy variables were the final on-therapy scores on the HAM-D, Montgomery-Asberg Depression Rating Scale and Clinical Global Impression severity scales. Data were evaluated on an intent-to-treat basis using the LOCF method. One hundred and 16 patients were randomized, and 115 were evaluated for efficacy. Both drugs showed efficacy in the treatment of depression with or without melancholia. No significant differences were noted between treatments for any efficacy parameter. However, significantly (p < 0.05) more patients in the amitriptyline group had at least one adverse event. These results should support the efficacy and tolerability of venlafaxine in comparison with amitriptyline for treating major depression with or without melancholia.en
dc.format.extent61-66-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAmitriptyline-
dc.subjectDepression-
dc.subjectMelancholia-
dc.subjectVenlafaxine-
dc.subjectamitriptyline-
dc.subjectvenlafaxine-
dc.subjectadult-
dc.subjectappetite disorder-
dc.subjectclinical trial-
dc.subjectconstipation-
dc.subjectcontrolled clinical trial-
dc.subjectcontrolled study-
dc.subjectdata analysis-
dc.subjectdepression-
dc.subjectdisease severity-
dc.subjectdouble blind procedure-
dc.subjectdrug efficacy-
dc.subjectdrug tolerability-
dc.subjectfemale-
dc.subjectHamilton scale-
dc.subjectheadache-
dc.subjecthuman-
dc.subjecthypertension-
dc.subjectinsomnia-
dc.subjectmajor clinical study-
dc.subjectmale-
dc.subjectmelancholia-
dc.subjectmulticenter study-
dc.subjectnausea-
dc.subjectoutpatient care-
dc.subjectparesthesia-
dc.subjectpriority journal-
dc.subjectrandomized controlled trial-
dc.subjectrash-
dc.subjectrating scale-
dc.subjectsomnolence-
dc.subjectsweating-
dc.subjectsymptom-
dc.subjecttaste disorder-
dc.subjecttremor-
dc.subjectvertigo-
dc.subjectvisual impairment-
dc.subjectxerostomia-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectAmbulatory Care-
dc.subjectAntidepressive Agents, Second-Generation-
dc.subjectAntidepressive Agents, Tricyclic-
dc.subjectCyclohexanols-
dc.subjectDepressive Disorder-
dc.subjectDepressive Disorder, Major-
dc.subjectDouble-Blind Method-
dc.subjectFemale-
dc.subjectHumans-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectPersonality Inventory-
dc.subjectTreatment Outcome-
dc.titleDouble-blind comparison of venlafaxine and amitriptyline in outpatients with major depression with or without melancholiaen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)-
dc.contributor.institutionUniversidade Federal de Goiás (UFG)-
dc.contributor.institutionLaboratórios Wyeth-
dc.description.affiliationUniversidade de São Paulo, São Paulo-
dc.description.affiliationUniv. do Estado de São Paulo, Botucatu-
dc.description.affiliationUniv. Federal do Rio Grande do Sul, Porto Alegre-
dc.description.affiliationUniversidade Federal de Goiás, Goiánia-
dc.description.affiliationLaboratórios Wyeth, São Paulo-
dc.description.affiliationDepartamento de Psiquiatria Instituto de Psiquiatria Universidade de São Paulo, Rua Dr Ovidio Pires de Campos s/n, 05403-010 São Paulo-
dc.identifier.doi10.1177/026988110001400108-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Psychopharmacology-
dc.identifier.scopus2-s2.0-0034021822-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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