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Nitrous oxide as an adjunctive therapy in major depressive disorder: a randomized controlled double-blind pilot trial
Guimarães, Mara C.; Guimarães, Tiago M.; Hallak, Jaime E.; Abrão, João; Machado-de-Sousa, João P..
  • Guimarães, Mara C.; Universidade de São Paulo (USP). Faculdade de Medicina de Ribeirão Preto. Departamento de Neurociências e Ciências do Comportamento. Ribeirão Preto. BR
  • Guimarães, Tiago M.; Universidade de São Paulo (USP). Faculdade de Medicina de Ribeirão Preto. Departamento de Neurociências e Ciências do Comportamento. Ribeirão Preto. BR
  • Hallak, Jaime E.; Universidade de São Paulo (USP). Faculdade de Medicina de Ribeirão Preto. Departamento de Neurociências e Ciências do Comportamento. Ribeirão Preto. BR
  • Abrão, João; USP. Faculdade de Medicina de Ribeirão Preto. Departamento de Ortopedia e Anestesiologia. Ribeirão Preto. BR
  • Machado-de-Sousa, João P.; Universidade de São Paulo (USP). Faculdade de Medicina de Ribeirão Preto. Departamento de Neurociências e Ciências do Comportamento. Ribeirão Preto. BR
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 43(5): 484-493, Sept.-Oct. 2021. tab, graf
Article in English | LILACS | ID: biblio-1345467
ABSTRACT

Objective:

Major depressive disorder (MDD) is related to glutamatergic dysfunction. Antagonists of glutamatergic N-methyl-D-aspartate receptor (NMDAR), such as ketamine, have antidepressant properties. Nitrous oxide (N2O) is also a NMDAR antagonist. Thus, this study aimed to evaluate the effects of augmenting antidepressant treatment with N2O.

Methods:

This double blind, placebo-controlled randomized parallel pilot trial was conducted from June 2016 to June 2018 at the Hospital das Clínicas, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Twenty-three subjects with MDD (aged 18 to 65, on antidepressants, with a score > 17 on the 17-item-Hamilton Depression Rating Scale [HAM-D17]) received 50% N2O (n=12; 37.17±13.59 years) or placebo (100% oxygen) (n=11; 37.18±12.77 years) for 60 minutes twice a week for 4 weeks. The primary outcome was changes in HAM-D17 from baseline to week 4.

Results:

Depressive symptoms improved significantly in the N2O group (N2O from 22.58±3.83 to 5.92±4.08; placebo from 22.44±3.54 to 12.89±5.39, p < 0.005). A total of 91.7% and 75% of the N2O group subjects achieved response (≥ 50% reduction in HAM-D17 score) and remission (HAM-D17 < 7), respectively. The predominant adverse effects of N2O treatment were nausea, vomiting, and headache.

Conclusion:

N2O treatment led to a statistically significant reduction in HAM-D17 scores compared to placebo. Clinical trial registration Brazilian Register of Clinical Trials, RBR-5rz5ch
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Depressive Disorder, Major Type of study: Controlled clinical trial Country/Region as subject: South America / Brazil Language: English Journal: Braz. J. Psychiatry (São Paulo, 1999, Impr.) Journal subject: Psychiatry Year: 2021 Type: Article Affiliation country: Brazil Institution/Affiliation country: USP/BR / Universidade de São Paulo (USP)/BR

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Full text: Available Index: LILACS (Americas) Main subject: Depressive Disorder, Major Type of study: Controlled clinical trial Country/Region as subject: South America / Brazil Language: English Journal: Braz. J. Psychiatry (São Paulo, 1999, Impr.) Journal subject: Psychiatry Year: 2021 Type: Article Affiliation country: Brazil Institution/Affiliation country: USP/BR / Universidade de São Paulo (USP)/BR