International Clinical Psychopharmacology · 2020 · 40 citations · 21 references
MedicinePharmacologyPsychiatryClinical PharmacologyPsychiatric PharmacotherapyPsychopharmacologyAntidepressant PharmacologyAntidepressant PharmacotherapyAntidepressant TherapyDepression ManagementDepression PharmacotherapyTreatment Outcome EvaluationAdverse Drug EventsAntidepressant EfficacyAntidepressant MedicationsAntidepressant ResponseAntidepressant SafetyDouble-blind TrialsPharmacotherapy For Late-life DepressionPrimary Efficacy Endpoints
This double-blind, randomized study evaluated the efficacy and safety of trazodone OAD (once-a-day) in comparison with venlafaxine XR (extended-release) in 324 patients (166 trazodone and 158 venlafaxine) with major depressive disorder (MDD). The primary efficacy endpoint was the mean change from baseline in the 17-item Hamilton Depression Rating Scale (HAM-D) at week 8. Both treatments were effective in reducing the HAM-D-17 total score at week 8 vs. baseline (intent-to-treat: trazodone -12.9, venlafaxine -14.7; per protocol: trazodone -15.4, venlafaxine -16.4). Patients in the venlafaxine group achieved better results after 8 weeks, whereas the trazodone group achieved a statistically significant reduction in HAM-D-17 following only 7 days of treatment. The most frequent adverse events (AEs) were dizziness and somnolence in the trazodone group, and nausea and headache in the venlafaxine group. Most AEs were mild-to-moderate in severity. This study confirmed that both venlafaxine XR and trazodone OAD may represent a valid treatment option for patients with MDD.
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Projections of Global Mortality and Burden of Disease from 2002 to 2030
Colin Mathers, Dejan Lončar · PLoS Medicine · 2006 · 11.5K citations · Full text
Sleep disorders as core symptoms of depression
David Nutt, Sue Wilson, Louise M. Paterson · Dialogues in Clinical Neuroscience · 2008 · 819 citations · Full text
Medicine, Psychiatry, Psychology +17