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Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients
The traditional Japanese (Kampo) medicine, kakkonto with shosaikotokakikyosekko, has antiviral and anti-inflammatory effects. In this randomized trial, patients with mild and moderate coronavirus disease (COVID-19) were randomly allocated to the control group receiving conventional treatment for sym...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682103/ https://www.ncbi.nlm.nih.gov/pubmed/36438822 http://dx.doi.org/10.3389/fphar.2022.1008946 |
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author | Takayama, Shin Namiki, Takao Arita, Ryutaro Ono, Rie Kikuchi, Akiko Ohsawa, Minoru Saito, Natsumi Suzuki, Satoko Nakae, Hajime Kobayashi, Seiichi Yoshino, Tetsuhiro Ishigami, Tomoaki Tanaka, Koichiro Nochioka, Kotaro Takagi, Airi Mimura, Masaru Yamaguchi, Takuhiro Ishii, Tadashi Hisanaga, Akito Mitani, Kazuo Ito, Takashi |
author_facet | Takayama, Shin Namiki, Takao Arita, Ryutaro Ono, Rie Kikuchi, Akiko Ohsawa, Minoru Saito, Natsumi Suzuki, Satoko Nakae, Hajime Kobayashi, Seiichi Yoshino, Tetsuhiro Ishigami, Tomoaki Tanaka, Koichiro Nochioka, Kotaro Takagi, Airi Mimura, Masaru Yamaguchi, Takuhiro Ishii, Tadashi Hisanaga, Akito Mitani, Kazuo Ito, Takashi |
author_sort | Takayama, Shin |
collection | PubMed |
description | The traditional Japanese (Kampo) medicine, kakkonto with shosaikotokakikyosekko, has antiviral and anti-inflammatory effects. In this randomized trial, patients with mild and moderate coronavirus disease (COVID-19) were randomly allocated to the control group receiving conventional treatment for symptom relief such as antipyretics and antitussives or the Kampo group receiving mixed extract granules of kakkonto (2.5 g) and shosaikotokakikyosekko (2.5 g) three times a day for 14 days in addition to conventional treatment. The main outcome was the number of days until total symptom relief. The secondary outcome was the number of days until each symptom’s relief and whether the disease progressed to respiratory failure. We enrolled a total of 161 patients (Kampo group, n = 81; control group, n = 80). The results from Kaplan–Meier estimates of symptom relief showed that there are no significant differences between the groups. However, covariate-adjusted cumulative incidence of fever relief considering competitive risk showed that the recovery was significantly faster in the Kampo group than in the control group (HR 1.76, 95% CI 1.03–3.01). Additionally, the risk of disease progression to moderate COVID-19 requiring oxygen inhalation was lower in the Kampo group than in the control group (Risk Difference −0.13, 95% CI −0.27–0.01). No significant drug-related side effects were observed. Kakkonto with shosaikotokakikyosekko is effective for fever relief with suppression of disease progression in COVID-19 patients. Clinical Trial Registration: https://jrct.niph.go.jp/en-latest-detail/jRCTs021200020, identifier [jRCTs021200020] |
format | Online Article Text |
id | pubmed-9682103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96821032022-11-24 Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients Takayama, Shin Namiki, Takao Arita, Ryutaro Ono, Rie Kikuchi, Akiko Ohsawa, Minoru Saito, Natsumi Suzuki, Satoko Nakae, Hajime Kobayashi, Seiichi Yoshino, Tetsuhiro Ishigami, Tomoaki Tanaka, Koichiro Nochioka, Kotaro Takagi, Airi Mimura, Masaru Yamaguchi, Takuhiro Ishii, Tadashi Hisanaga, Akito Mitani, Kazuo Ito, Takashi Front Pharmacol Pharmacology The traditional Japanese (Kampo) medicine, kakkonto with shosaikotokakikyosekko, has antiviral and anti-inflammatory effects. In this randomized trial, patients with mild and moderate coronavirus disease (COVID-19) were randomly allocated to the control group receiving conventional treatment for symptom relief such as antipyretics and antitussives or the Kampo group receiving mixed extract granules of kakkonto (2.5 g) and shosaikotokakikyosekko (2.5 g) three times a day for 14 days in addition to conventional treatment. The main outcome was the number of days until total symptom relief. The secondary outcome was the number of days until each symptom’s relief and whether the disease progressed to respiratory failure. We enrolled a total of 161 patients (Kampo group, n = 81; control group, n = 80). The results from Kaplan–Meier estimates of symptom relief showed that there are no significant differences between the groups. However, covariate-adjusted cumulative incidence of fever relief considering competitive risk showed that the recovery was significantly faster in the Kampo group than in the control group (HR 1.76, 95% CI 1.03–3.01). Additionally, the risk of disease progression to moderate COVID-19 requiring oxygen inhalation was lower in the Kampo group than in the control group (Risk Difference −0.13, 95% CI −0.27–0.01). No significant drug-related side effects were observed. Kakkonto with shosaikotokakikyosekko is effective for fever relief with suppression of disease progression in COVID-19 patients. Clinical Trial Registration: https://jrct.niph.go.jp/en-latest-detail/jRCTs021200020, identifier [jRCTs021200020] Frontiers Media S.A. 2022-11-09 /pmc/articles/PMC9682103/ /pubmed/36438822 http://dx.doi.org/10.3389/fphar.2022.1008946 Text en Copyright © 2022 Takayama, Namiki, Arita, Ono, Kikuchi, Ohsawa, Saito, Suzuki, Nakae, Kobayashi, Yoshino, Ishigami, Tanaka, Nochioka, Takagi, Mimura, Yamaguchi, Ishii, Hisanaga, Mitani and Ito. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Takayama, Shin Namiki, Takao Arita, Ryutaro Ono, Rie Kikuchi, Akiko Ohsawa, Minoru Saito, Natsumi Suzuki, Satoko Nakae, Hajime Kobayashi, Seiichi Yoshino, Tetsuhiro Ishigami, Tomoaki Tanaka, Koichiro Nochioka, Kotaro Takagi, Airi Mimura, Masaru Yamaguchi, Takuhiro Ishii, Tadashi Hisanaga, Akito Mitani, Kazuo Ito, Takashi Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
title | Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
title_full | Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
title_fullStr | Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
title_full_unstemmed | Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
title_short | Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
title_sort | multicenter, randomized controlled trial of traditional japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682103/ https://www.ncbi.nlm.nih.gov/pubmed/36438822 http://dx.doi.org/10.3389/fphar.2022.1008946 |
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