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The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke

Background: HuatuoZaizao pill (HZP), a Chinese patent medicine, is often used in the treatment of stroke. However, there is still a lack of enough evidence to recommend the routine use of HZP for stroke. This study is aimed at evaluating the quality of reporting of randomized controlled trials (RCTs...

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Autores principales: Zhang, Xiao-Jie, Wang, Yi-Jing, Lu, Xiao, Ying, Peng-Jie, Qian, Shi-Yan, Liang, Jie, Zheng, Guo-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871376/
https://www.ncbi.nlm.nih.gov/pubmed/36703753
http://dx.doi.org/10.3389/fphar.2022.1106957
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author Zhang, Xiao-Jie
Wang, Yi-Jing
Lu, Xiao
Ying, Peng-Jie
Qian, Shi-Yan
Liang, Jie
Zheng, Guo-Qing
author_facet Zhang, Xiao-Jie
Wang, Yi-Jing
Lu, Xiao
Ying, Peng-Jie
Qian, Shi-Yan
Liang, Jie
Zheng, Guo-Qing
author_sort Zhang, Xiao-Jie
collection PubMed
description Background: HuatuoZaizao pill (HZP), a Chinese patent medicine, is often used in the treatment of stroke. However, there is still a lack of enough evidence to recommend the routine use of HZP for stroke. This study is aimed at evaluating the quality of reporting of randomized controlled trials (RCTs) on HZP for stroke. Methods: RCTs on HuatuoZaizao pill for stroke were evaluated by using Consolidated Standards of Reporting Trials (CONSORT) guidelines and CONSORT extension criteria on reporting herbal interventions (CONSORT-CHM) guidelines. Microsoft Excel 2007 and SPSS20.0 was used for statistics analyses. Results: Seventeen studies involving 1801 stroke patients were identified. CONSORT-CHM has expanded 24.3% (9/37) items in CONSORT and added a small item. The average scores of CONSORT evaluation is 14.6, while the average scores of the CONSORT-CHM evaluation is 11.6. The central items in CONSORT as eligibility criterion, sample size calculation, primary outcome, method of randomization sequence generation, allocation concealment, implementation of randomization, description of blinding, and detailed statistical methods were reported in 77%, 6%, 100%, 47%, 6%, 6%, 6%, and 94% of trials, respectively. In terms of the CONSORT-CHM, none of the articles reported in detail the dosage form, origin, formula basis and so on of HZP, and only half of studies reported the outcome indicators related to Traditional Chinese Medicine syndromes. Conclusion: The overall report quality of RCT related to HZP is low. HZP still needs to report higher quality RCTs to prove its effectiveness and safety.
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spelling pubmed-98713762023-01-25 The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke Zhang, Xiao-Jie Wang, Yi-Jing Lu, Xiao Ying, Peng-Jie Qian, Shi-Yan Liang, Jie Zheng, Guo-Qing Front Pharmacol Pharmacology Background: HuatuoZaizao pill (HZP), a Chinese patent medicine, is often used in the treatment of stroke. However, there is still a lack of enough evidence to recommend the routine use of HZP for stroke. This study is aimed at evaluating the quality of reporting of randomized controlled trials (RCTs) on HZP for stroke. Methods: RCTs on HuatuoZaizao pill for stroke were evaluated by using Consolidated Standards of Reporting Trials (CONSORT) guidelines and CONSORT extension criteria on reporting herbal interventions (CONSORT-CHM) guidelines. Microsoft Excel 2007 and SPSS20.0 was used for statistics analyses. Results: Seventeen studies involving 1801 stroke patients were identified. CONSORT-CHM has expanded 24.3% (9/37) items in CONSORT and added a small item. The average scores of CONSORT evaluation is 14.6, while the average scores of the CONSORT-CHM evaluation is 11.6. The central items in CONSORT as eligibility criterion, sample size calculation, primary outcome, method of randomization sequence generation, allocation concealment, implementation of randomization, description of blinding, and detailed statistical methods were reported in 77%, 6%, 100%, 47%, 6%, 6%, 6%, and 94% of trials, respectively. In terms of the CONSORT-CHM, none of the articles reported in detail the dosage form, origin, formula basis and so on of HZP, and only half of studies reported the outcome indicators related to Traditional Chinese Medicine syndromes. Conclusion: The overall report quality of RCT related to HZP is low. HZP still needs to report higher quality RCTs to prove its effectiveness and safety. Frontiers Media S.A. 2023-01-10 /pmc/articles/PMC9871376/ /pubmed/36703753 http://dx.doi.org/10.3389/fphar.2022.1106957 Text en Copyright © 2023 Zhang, Wang, Lu, Ying, Qian, Liang and Zheng. 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
Zhang, Xiao-Jie
Wang, Yi-Jing
Lu, Xiao
Ying, Peng-Jie
Qian, Shi-Yan
Liang, Jie
Zheng, Guo-Qing
The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke
title The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke
title_full The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke
title_fullStr The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke
title_full_unstemmed The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke
title_short The quality of reporting of randomized controlled trials of HuatuoZaizao pill for stroke
title_sort quality of reporting of randomized controlled trials of huatuozaizao pill for stroke
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871376/
https://www.ncbi.nlm.nih.gov/pubmed/36703753
http://dx.doi.org/10.3389/fphar.2022.1106957
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