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A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss

BACKGROUND: Hydrogen (H(2)) has been reported to be effective in reducing hearing loss due to several causes in animal studies. However, no study has examined the effectiveness of H(2) in treating hearing loss in humans. Thus, we investigated whether H(2) is effective for the treatment of idiopathic...

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Autores principales: Okada, Masahiro, Ogawa, Hideo, Takagi, Taro, Nishihara, Eriko, Yoshida, Tadashi, Hyodo, Jun, Shinomori, Yusuke, Honda, Nobumitsu, Fujiwara, Takashi, Teraoka, Masato, Yamada, Hiroyuki, Hirano, Shin-ichi, Hato, Naohito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731512/
https://www.ncbi.nlm.nih.gov/pubmed/36507329
http://dx.doi.org/10.3389/fnins.2022.1024634
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author Okada, Masahiro
Ogawa, Hideo
Takagi, Taro
Nishihara, Eriko
Yoshida, Tadashi
Hyodo, Jun
Shinomori, Yusuke
Honda, Nobumitsu
Fujiwara, Takashi
Teraoka, Masato
Yamada, Hiroyuki
Hirano, Shin-ichi
Hato, Naohito
author_facet Okada, Masahiro
Ogawa, Hideo
Takagi, Taro
Nishihara, Eriko
Yoshida, Tadashi
Hyodo, Jun
Shinomori, Yusuke
Honda, Nobumitsu
Fujiwara, Takashi
Teraoka, Masato
Yamada, Hiroyuki
Hirano, Shin-ichi
Hato, Naohito
author_sort Okada, Masahiro
collection PubMed
description BACKGROUND: Hydrogen (H(2)) has been reported to be effective in reducing hearing loss due to several causes in animal studies. However, no study has examined the effectiveness of H(2) in treating hearing loss in humans. Thus, we investigated whether H(2) is effective for the treatment of idiopathic sudden sensorineural hearing loss (ISSNHL). MATERIALS AND METHODS: We conducted a double-blind randomized controlled trial at six hospitals between June 2019 and March 2022. The study protocol and trial registration have been published in the Japan Registry of Clinical Trials (jRCT, No. jRCTs06119004). We randomly assigned patients with ISSNHL to receive either H(2) (H(2) group) or air as a placebo (control group) through inhalation combined with the administration of systemic glucocorticoids and prostaglandin E1. The primary outcome was the hearing threshold and changes in hearing threshold 3 months after therapy. In contrast, the secondary outcomes included the proportion of patients with a good prognosis (complete recovery or marked improvement). RESULTS: Sixty-five patients with ISSNHL (31 and 34 in the H(2) and control groups, respectively) were included in this study. The hearing threshold 3 months after treatment was not significantly different between the groups; 39.0 decibels (dB) (95% confidence interval [CI]: 28.7–49.3) and 49.5 dB (95% CI: 40.3–58.7) in the H(2) and control groups, respectively. In contrast, the changes in hearing threshold 3 months after treatment was 32.7 dB (95% CI: 24.2–41.3) and 24.2 dB (95% CI: 18.1–30.3) in the H(2) and control groups, respectively. Consequently, the changes in hearing threshold were significantly better in the H(2) group than in the control group (P = 0.048). However, no adverse effects due to the inhalation of H(2) gas have been reported. CONCLUSION: This is the first study to investigate the efficacy of H(2) for the treatment of ISSNHL in humans. The results suggest that H(2) therapy may be effective for ISSNHL treatment. CLINICAL TRIAL REGISTRATION: [https://jrct.niph.go.jp/re/reports/detail/10442], identifier [jRCTs06119004].
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spelling pubmed-97315122022-12-09 A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss Okada, Masahiro Ogawa, Hideo Takagi, Taro Nishihara, Eriko Yoshida, Tadashi Hyodo, Jun Shinomori, Yusuke Honda, Nobumitsu Fujiwara, Takashi Teraoka, Masato Yamada, Hiroyuki Hirano, Shin-ichi Hato, Naohito Front Neurosci Neuroscience BACKGROUND: Hydrogen (H(2)) has been reported to be effective in reducing hearing loss due to several causes in animal studies. However, no study has examined the effectiveness of H(2) in treating hearing loss in humans. Thus, we investigated whether H(2) is effective for the treatment of idiopathic sudden sensorineural hearing loss (ISSNHL). MATERIALS AND METHODS: We conducted a double-blind randomized controlled trial at six hospitals between June 2019 and March 2022. The study protocol and trial registration have been published in the Japan Registry of Clinical Trials (jRCT, No. jRCTs06119004). We randomly assigned patients with ISSNHL to receive either H(2) (H(2) group) or air as a placebo (control group) through inhalation combined with the administration of systemic glucocorticoids and prostaglandin E1. The primary outcome was the hearing threshold and changes in hearing threshold 3 months after therapy. In contrast, the secondary outcomes included the proportion of patients with a good prognosis (complete recovery or marked improvement). RESULTS: Sixty-five patients with ISSNHL (31 and 34 in the H(2) and control groups, respectively) were included in this study. The hearing threshold 3 months after treatment was not significantly different between the groups; 39.0 decibels (dB) (95% confidence interval [CI]: 28.7–49.3) and 49.5 dB (95% CI: 40.3–58.7) in the H(2) and control groups, respectively. In contrast, the changes in hearing threshold 3 months after treatment was 32.7 dB (95% CI: 24.2–41.3) and 24.2 dB (95% CI: 18.1–30.3) in the H(2) and control groups, respectively. Consequently, the changes in hearing threshold were significantly better in the H(2) group than in the control group (P = 0.048). However, no adverse effects due to the inhalation of H(2) gas have been reported. CONCLUSION: This is the first study to investigate the efficacy of H(2) for the treatment of ISSNHL in humans. The results suggest that H(2) therapy may be effective for ISSNHL treatment. CLINICAL TRIAL REGISTRATION: [https://jrct.niph.go.jp/re/reports/detail/10442], identifier [jRCTs06119004]. Frontiers Media S.A. 2022-11-24 /pmc/articles/PMC9731512/ /pubmed/36507329 http://dx.doi.org/10.3389/fnins.2022.1024634 Text en Copyright © 2022 Okada, Ogawa, Takagi, Nishihara, Yoshida, Hyodo, Shinomori, Honda, Fujiwara, Teraoka, Yamada, Hirano and Hato. 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 Neuroscience
Okada, Masahiro
Ogawa, Hideo
Takagi, Taro
Nishihara, Eriko
Yoshida, Tadashi
Hyodo, Jun
Shinomori, Yusuke
Honda, Nobumitsu
Fujiwara, Takashi
Teraoka, Masato
Yamada, Hiroyuki
Hirano, Shin-ichi
Hato, Naohito
A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
title A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
title_full A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
title_fullStr A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
title_full_unstemmed A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
title_short A double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
title_sort double-blinded, randomized controlled clinical trial of hydrogen inhalation therapy for idiopathic sudden sensorineural hearing loss
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731512/
https://www.ncbi.nlm.nih.gov/pubmed/36507329
http://dx.doi.org/10.3389/fnins.2022.1024634
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