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Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome

Objective. To explore the efficacy of Herb-partitioned moxibustion in treating IBS-D patients. Method. 210 IBS-D patients were randomly assigned on a 3 : 3 : 2 basis to group HM, group FM, or group PB for 4-week treatment. The change of GSRS total score at weeks 4 and 8, the changes of GSRS specific...

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Autores principales: Ma, Yu-xia, Liu, Xiao, Liu, Cun-zhi, Wang, Lin-peng, Guo, Gang, Du, Dong-qing, Wang, Zhi-lei, Ma, Hong, Qi, Ping, Li, Zhao-feng, Guo, Yan-ping, Yi, Hua-qiang, Gao, Shu-zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880695/
https://www.ncbi.nlm.nih.gov/pubmed/24454500
http://dx.doi.org/10.1155/2013/605460
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author Ma, Yu-xia
Liu, Xiao
Liu, Cun-zhi
Wang, Lin-peng
Guo, Gang
Du, Dong-qing
Wang, Zhi-lei
Ma, Hong
Qi, Ping
Li, Zhao-feng
Guo, Yan-ping
Yi, Hua-qiang
Gao, Shu-zhong
author_facet Ma, Yu-xia
Liu, Xiao
Liu, Cun-zhi
Wang, Lin-peng
Guo, Gang
Du, Dong-qing
Wang, Zhi-lei
Ma, Hong
Qi, Ping
Li, Zhao-feng
Guo, Yan-ping
Yi, Hua-qiang
Gao, Shu-zhong
author_sort Ma, Yu-xia
collection PubMed
description Objective. To explore the efficacy of Herb-partitioned moxibustion in treating IBS-D patients. Method. 210 IBS-D patients were randomly assigned on a 3 : 3 : 2 basis to group HM, group FM, or group PB for 4-week treatment. The change of GSRS total score at weeks 4 and 8, the changes of GSRS specific scores, and adverse events were evaluated. Results. Patients in group HM and group FM had lower GSRS total score at week 4 (1.98 ± 0.303, 2.93 ± 0.302 versus 3.73 ± 0.449) and at week 8 (2.75 ± 0.306, 3.56 ± 0.329 versus 4.39 ± 2.48) as compared with patients' score in group PB. However, there was no significant difference of GSRS total score between group HM and group FM. The effect of HM was significantly greater than that of orally taking PB in ameliorating the symptoms of rugitus (0.38 versus 0.59, P < 0.05), abdominal pain (0.28 versus 0.57, P < 0.01), abdominal distension (0.4 versus 0.7, P < 0.01), and increased passage of stools (0.06 versus 0.25, P < 0.01) at the end of treatment period. In the follow-up period, patients' therapeutic effect in group HM remained greater than that in group FM (in abdominal pain, abdominal distension, and increased passage of stools) and that in group PB (in loose stools). Conclusions. HM appears to be a promising, efficacious, and well-tolerated treatment for patients with IBS-D.
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spelling pubmed-38806952014-01-20 Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome Ma, Yu-xia Liu, Xiao Liu, Cun-zhi Wang, Lin-peng Guo, Gang Du, Dong-qing Wang, Zhi-lei Ma, Hong Qi, Ping Li, Zhao-feng Guo, Yan-ping Yi, Hua-qiang Gao, Shu-zhong Evid Based Complement Alternat Med Research Article Objective. To explore the efficacy of Herb-partitioned moxibustion in treating IBS-D patients. Method. 210 IBS-D patients were randomly assigned on a 3 : 3 : 2 basis to group HM, group FM, or group PB for 4-week treatment. The change of GSRS total score at weeks 4 and 8, the changes of GSRS specific scores, and adverse events were evaluated. Results. Patients in group HM and group FM had lower GSRS total score at week 4 (1.98 ± 0.303, 2.93 ± 0.302 versus 3.73 ± 0.449) and at week 8 (2.75 ± 0.306, 3.56 ± 0.329 versus 4.39 ± 2.48) as compared with patients' score in group PB. However, there was no significant difference of GSRS total score between group HM and group FM. The effect of HM was significantly greater than that of orally taking PB in ameliorating the symptoms of rugitus (0.38 versus 0.59, P < 0.05), abdominal pain (0.28 versus 0.57, P < 0.01), abdominal distension (0.4 versus 0.7, P < 0.01), and increased passage of stools (0.06 versus 0.25, P < 0.01) at the end of treatment period. In the follow-up period, patients' therapeutic effect in group HM remained greater than that in group FM (in abdominal pain, abdominal distension, and increased passage of stools) and that in group PB (in loose stools). Conclusions. HM appears to be a promising, efficacious, and well-tolerated treatment for patients with IBS-D. Hindawi Publishing Corporation 2013 2013-12-19 /pmc/articles/PMC3880695/ /pubmed/24454500 http://dx.doi.org/10.1155/2013/605460 Text en Copyright © 2013 Yu-xia Ma et al. https://creativecommons.org/licenses/by/3.0/ 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
Ma, Yu-xia
Liu, Xiao
Liu, Cun-zhi
Wang, Lin-peng
Guo, Gang
Du, Dong-qing
Wang, Zhi-lei
Ma, Hong
Qi, Ping
Li, Zhao-feng
Guo, Yan-ping
Yi, Hua-qiang
Gao, Shu-zhong
Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome
title Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome
title_full Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome
title_fullStr Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome
title_full_unstemmed Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome
title_short Randomized Clinical Trial: The Clinical Effects of Herb-Partitioned Moxibustion in Patients with Diarrhoea-Predominant Irritable Bowel Syndrome
title_sort randomized clinical trial: the clinical effects of herb-partitioned moxibustion in patients with diarrhoea-predominant irritable bowel syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880695/
https://www.ncbi.nlm.nih.gov/pubmed/24454500
http://dx.doi.org/10.1155/2013/605460
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