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A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression

BACKGROUND: Depressive disorders are considered to be one of the leading causes of morbidity and mortality accounting for 4.3% of total disability-adjusted life years. Selective serotonin reuptake inhibitors and serotonin–norepinephrine reuptake inhibitors have greater efficacy and lesser side effec...

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Autores principales: Bathla, Manish, Anjum, Shazia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074431/
https://www.ncbi.nlm.nih.gov/pubmed/32201441
http://dx.doi.org/10.4103/ijp.IJP_618_18
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author Bathla, Manish
Anjum, Shazia
author_facet Bathla, Manish
Anjum, Shazia
author_sort Bathla, Manish
collection PubMed
description BACKGROUND: Depressive disorders are considered to be one of the leading causes of morbidity and mortality accounting for 4.3% of total disability-adjusted life years. Selective serotonin reuptake inhibitors and serotonin–norepinephrine reuptake inhibitors have greater efficacy and lesser side effects; at the same time, these drugs cause sexual dysfunction and weight gain. Vilazodone was supposed to have better efficacy and less sexual dysfunction and weight gain. AIM OF THE STUDY: The aim is to compare efficacy (in terms of Hamilton Depression Rating Scale [HDRS]), sexual dysfunction (in terms of Arizona Sexual Experience Scale [ASEX]), and weight gain caused due to vilazodone and sertraline. MATERIALS AND METHODS: This is a randomized controlled study; 60 patients diagnosed with depressive episode were divided into two groups of 30 each; using block randomization technique, one group was prescribed vilazodone and another sertraline. The groups were compared on the basis of efficacy, weight gain, and sexual dysfunction using HDRS and ASEX at baseline, 4-week, and 12-week intervals. Statistical analysis was done by applying Chi-square test, Fisher's exact test, t-test, and repeated measures ANOVA using Wilks' lambda test. RESULTS: On comparing both vilazodone and sertraline, it was observed that both molecules have equal efficacy in terms of HDRS, but vilazodone does not cause weight gain and sexual dysfunction in terms of ASEX, and these findings are statistically very highly significant. CONCLUSIONS: Our study shows that vilazodone has similar efficacy but can be a better antidepressant due to lesser weight gain and sexual dysfunction compared to sertraline.
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spelling pubmed-70744312020-03-20 A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression Bathla, Manish Anjum, Shazia Indian J Pharmacol Research Article BACKGROUND: Depressive disorders are considered to be one of the leading causes of morbidity and mortality accounting for 4.3% of total disability-adjusted life years. Selective serotonin reuptake inhibitors and serotonin–norepinephrine reuptake inhibitors have greater efficacy and lesser side effects; at the same time, these drugs cause sexual dysfunction and weight gain. Vilazodone was supposed to have better efficacy and less sexual dysfunction and weight gain. AIM OF THE STUDY: The aim is to compare efficacy (in terms of Hamilton Depression Rating Scale [HDRS]), sexual dysfunction (in terms of Arizona Sexual Experience Scale [ASEX]), and weight gain caused due to vilazodone and sertraline. MATERIALS AND METHODS: This is a randomized controlled study; 60 patients diagnosed with depressive episode were divided into two groups of 30 each; using block randomization technique, one group was prescribed vilazodone and another sertraline. The groups were compared on the basis of efficacy, weight gain, and sexual dysfunction using HDRS and ASEX at baseline, 4-week, and 12-week intervals. Statistical analysis was done by applying Chi-square test, Fisher's exact test, t-test, and repeated measures ANOVA using Wilks' lambda test. RESULTS: On comparing both vilazodone and sertraline, it was observed that both molecules have equal efficacy in terms of HDRS, but vilazodone does not cause weight gain and sexual dysfunction in terms of ASEX, and these findings are statistically very highly significant. CONCLUSIONS: Our study shows that vilazodone has similar efficacy but can be a better antidepressant due to lesser weight gain and sexual dysfunction compared to sertraline. Wolters Kluwer - Medknow 2020 2020-03-11 /pmc/articles/PMC7074431/ /pubmed/32201441 http://dx.doi.org/10.4103/ijp.IJP_618_18 Text en Copyright: © 2020 Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Bathla, Manish
Anjum, Shazia
A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression
title A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression
title_full A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression
title_fullStr A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression
title_full_unstemmed A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression
title_short A 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in Indian patients with depression
title_sort 12-week prospective randomized controlled comparative trial of vilazodone and sertraline in indian patients with depression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074431/
https://www.ncbi.nlm.nih.gov/pubmed/32201441
http://dx.doi.org/10.4103/ijp.IJP_618_18
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