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Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial
BACKGROUND: Cough variant asthma (CVA) is one of the leading causes of chronic coughing. The main treatment is currently anti-inflammatory medication. However, the coughing may return or be aggravated and lung function may deteriorate once the anti-inflammatory treatment is stopped. The effect of Ch...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318874/ https://www.ncbi.nlm.nih.gov/pubmed/30606237 http://dx.doi.org/10.1186/s13063-018-3073-x |
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author | Fan, Rong-rong Wen, Ze-huai Wang, Da-wei Yang, Rong-yuan Ou, Ai-hua Jin, Lian-shun Zhang, Zhong-de Liu, Yun-tao |
author_facet | Fan, Rong-rong Wen, Ze-huai Wang, Da-wei Yang, Rong-yuan Ou, Ai-hua Jin, Lian-shun Zhang, Zhong-de Liu, Yun-tao |
author_sort | Fan, Rong-rong |
collection | PubMed |
description | BACKGROUND: Cough variant asthma (CVA) is one of the leading causes of chronic coughing. The main treatment is currently anti-inflammatory medication. However, the coughing may return or be aggravated and lung function may deteriorate once the anti-inflammatory treatment is stopped. The effect of Chinese herbal medicine (CHM) on chronic coughing is remarkable, but high-quality evidence supporting its effectiveness is still lacking. This trial aims to evaluate the safety and efficacy, especially the long-term efficacy, of CHM plus anti-inflammatory medications for the treatment of CVA. METHODS/DESIGN: A randomized placebo-controlled double-blind trial will be conducted. It will consist of a 3-month intervention followed by a 6-month follow-up period. The target sample size is 60 patients with CVA who are between 18 and 70 years old. The eligible subjects will be allocated randomly into the experimental or control group in a ratio of 1:1. Patients in the experimental group will take CHM granules (4.9 g twice daily), while patients in the control group will be given a matched placebo. An administration of salmeterol/fluticasone propionate combination for 12 weeks will be the basic therapy for the two groups. The primary outcome is the cough visual analog scales (CVAS). The secondary outcomes include quality of life, rate of symptom relapse, lung function, and blood tests. A safety assessment will also be performed during the trial. DISCUSSION: The evidence gathered by the trial will be a valuable addition to informing treatment options for patients with CVA. TRIAL REGISTRATION: http://www.chictr.org.cn, ID: ChiCTR-IOR-16009148. Registered on 3 September 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-3073-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6318874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63188742019-01-08 Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial Fan, Rong-rong Wen, Ze-huai Wang, Da-wei Yang, Rong-yuan Ou, Ai-hua Jin, Lian-shun Zhang, Zhong-de Liu, Yun-tao Trials Study Protocol BACKGROUND: Cough variant asthma (CVA) is one of the leading causes of chronic coughing. The main treatment is currently anti-inflammatory medication. However, the coughing may return or be aggravated and lung function may deteriorate once the anti-inflammatory treatment is stopped. The effect of Chinese herbal medicine (CHM) on chronic coughing is remarkable, but high-quality evidence supporting its effectiveness is still lacking. This trial aims to evaluate the safety and efficacy, especially the long-term efficacy, of CHM plus anti-inflammatory medications for the treatment of CVA. METHODS/DESIGN: A randomized placebo-controlled double-blind trial will be conducted. It will consist of a 3-month intervention followed by a 6-month follow-up period. The target sample size is 60 patients with CVA who are between 18 and 70 years old. The eligible subjects will be allocated randomly into the experimental or control group in a ratio of 1:1. Patients in the experimental group will take CHM granules (4.9 g twice daily), while patients in the control group will be given a matched placebo. An administration of salmeterol/fluticasone propionate combination for 12 weeks will be the basic therapy for the two groups. The primary outcome is the cough visual analog scales (CVAS). The secondary outcomes include quality of life, rate of symptom relapse, lung function, and blood tests. A safety assessment will also be performed during the trial. DISCUSSION: The evidence gathered by the trial will be a valuable addition to informing treatment options for patients with CVA. TRIAL REGISTRATION: http://www.chictr.org.cn, ID: ChiCTR-IOR-16009148. Registered on 3 September 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-3073-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-03 /pmc/articles/PMC6318874/ /pubmed/30606237 http://dx.doi.org/10.1186/s13063-018-3073-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Fan, Rong-rong Wen, Ze-huai Wang, Da-wei Yang, Rong-yuan Ou, Ai-hua Jin, Lian-shun Zhang, Zhong-de Liu, Yun-tao Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
title | Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
title_full | Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
title_fullStr | Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
title_full_unstemmed | Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
title_short | Chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
title_sort | chinese herbal medicine for the treatment of cough variant asthma: a study protocol for a double-blind randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318874/ https://www.ncbi.nlm.nih.gov/pubmed/30606237 http://dx.doi.org/10.1186/s13063-018-3073-x |
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