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Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial

BACKGROUND: Western drugs effectively manage persistent depressive disorder (PDD) but are associated with side effects. OBJECTIVE: To observe the efficacy and safety of modified Xiaochaihu Decoction combined with mirtazapine in treating PDD. METHODS: Patients with PDD were enrolled at the Naval Gene...

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Autores principales: Li, Xin, Li, Xiuyu, Gong, Man, Li, Chaoqun, Li, Jing, Zhou, Chao, He, Tingting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252686/
https://www.ncbi.nlm.nih.gov/pubmed/35833082
http://dx.doi.org/10.1155/2022/8682612
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author Li, Xin
Li, Xiuyu
Gong, Man
Li, Chaoqun
Li, Jing
Zhou, Chao
He, Tingting
author_facet Li, Xin
Li, Xiuyu
Gong, Man
Li, Chaoqun
Li, Jing
Zhou, Chao
He, Tingting
author_sort Li, Xin
collection PubMed
description BACKGROUND: Western drugs effectively manage persistent depressive disorder (PDD) but are associated with side effects. OBJECTIVE: To observe the efficacy and safety of modified Xiaochaihu Decoction combined with mirtazapine in treating PDD. METHODS: Patients with PDD were enrolled at the Naval General Hospital (06/2018–02/2019) and randomized to modified Xiaochaihu Decoction and modified Xiaochaihu Decoction with mirtazapine. The self-rating depression scale (SDS) and traditional Chinese medicine (TCM) scale were assessed at baseline and after 12 weeks. The overall clinical efficacy (primary outcome) and adverse reactions were observed. RESULTS: Sixty-four participants completed the trial in the combined and control groups (30 and 28), respectively. In controls, the total effective rate was 78.6%, compared with 96.7% in the combined group (P=0.035). The scores of the SDS and TCM syndrome scale in the two groups were lower after treatment (P < 0.001) but without difference between groups (P=0.077). The combined group showed higher improvement rates regarding insomnia (96.4% vs. 44.0%, P < 0.001), bitter taste (90.5% vs. 52.6%, P=0.007), languid (72.0% vs. 31.8%, P=0.006), and belching/anorexia (100% vs. 52.6%, P < 0.001). The combined group showed a higher frequency of adverse events (73.3% vs. 3.6%) (P < 0.001). CONCLUSION: Modified Xiaochaihu Decoction combined with mirtazapine effectively treats PDD, and its curative effect is better than that of TCM alone. Trial Registration. This trial was registered with https://www.chictr.org.cn/index.aspx/ChiCTR2100048188.
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spelling pubmed-92526862022-07-12 Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial Li, Xin Li, Xiuyu Gong, Man Li, Chaoqun Li, Jing Zhou, Chao He, Tingting Contrast Media Mol Imaging Research Article BACKGROUND: Western drugs effectively manage persistent depressive disorder (PDD) but are associated with side effects. OBJECTIVE: To observe the efficacy and safety of modified Xiaochaihu Decoction combined with mirtazapine in treating PDD. METHODS: Patients with PDD were enrolled at the Naval General Hospital (06/2018–02/2019) and randomized to modified Xiaochaihu Decoction and modified Xiaochaihu Decoction with mirtazapine. The self-rating depression scale (SDS) and traditional Chinese medicine (TCM) scale were assessed at baseline and after 12 weeks. The overall clinical efficacy (primary outcome) and adverse reactions were observed. RESULTS: Sixty-four participants completed the trial in the combined and control groups (30 and 28), respectively. In controls, the total effective rate was 78.6%, compared with 96.7% in the combined group (P=0.035). The scores of the SDS and TCM syndrome scale in the two groups were lower after treatment (P < 0.001) but without difference between groups (P=0.077). The combined group showed higher improvement rates regarding insomnia (96.4% vs. 44.0%, P < 0.001), bitter taste (90.5% vs. 52.6%, P=0.007), languid (72.0% vs. 31.8%, P=0.006), and belching/anorexia (100% vs. 52.6%, P < 0.001). The combined group showed a higher frequency of adverse events (73.3% vs. 3.6%) (P < 0.001). CONCLUSION: Modified Xiaochaihu Decoction combined with mirtazapine effectively treats PDD, and its curative effect is better than that of TCM alone. Trial Registration. This trial was registered with https://www.chictr.org.cn/index.aspx/ChiCTR2100048188. Hindawi 2022-06-27 /pmc/articles/PMC9252686/ /pubmed/35833082 http://dx.doi.org/10.1155/2022/8682612 Text en Copyright © 2022 Xin Li et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Xin
Li, Xiuyu
Gong, Man
Li, Chaoqun
Li, Jing
Zhou, Chao
He, Tingting
Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial
title Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial
title_full Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial
title_fullStr Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial
title_full_unstemmed Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial
title_short Modified Xiaochaihu Decoction Combined with Mirtazapine in the Treatment of Persistent Depression: A Pilot Randomized Controlled Trial
title_sort modified xiaochaihu decoction combined with mirtazapine in the treatment of persistent depression: a pilot randomized controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252686/
https://www.ncbi.nlm.nih.gov/pubmed/35833082
http://dx.doi.org/10.1155/2022/8682612
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