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Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial

INTRODUCTION: Patients with incomplete revascularization (ICR) tend to develop refractory angina despite optimal medical therapy. The Compound Danshen Dripping Pills (CDDP) is a widely used antianginal drug in China and is shown to significantly alleviate myocardial ischemia. Previous studies showed...

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Autores principales: Wu, Zexuan, Xu, Danping, Wu, Zhen, Chen, Ailan, Liu, Lijuan, Ling, Li, Zhou, Yan, Liu, Duoduo, Liu, Yin, Dong, Yugang, Chen, Yili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088738/
https://www.ncbi.nlm.nih.gov/pubmed/35557513
http://dx.doi.org/10.3389/fcvm.2022.860059
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author Wu, Zexuan
Xu, Danping
Wu, Zhen
Chen, Ailan
Liu, Lijuan
Ling, Li
Zhou, Yan
Liu, Duoduo
Liu, Yin
Dong, Yugang
Chen, Yili
author_facet Wu, Zexuan
Xu, Danping
Wu, Zhen
Chen, Ailan
Liu, Lijuan
Ling, Li
Zhou, Yan
Liu, Duoduo
Liu, Yin
Dong, Yugang
Chen, Yili
author_sort Wu, Zexuan
collection PubMed
description INTRODUCTION: Patients with incomplete revascularization (ICR) tend to develop refractory angina despite optimal medical therapy. The Compound Danshen Dripping Pills (CDDP) is a widely used antianginal drug in China and is shown to significantly alleviate myocardial ischemia. Previous studies showed dose-efficacy tendency when increasing doses of CDDP. This study aims to investigate the efficacy and safety of intensive doses of CDDP in patients with refractory angina with ICR. METHODS AND ANALYSIS: The INCODER study is a multicenter, double-blind, randomized controlled, superiority trial. We plan to recruit 250 patients aged 18–85 years with a diagnosis of refractory angina with ICR. Patients will be randomized (1:1) to intensive treatment group (CDDP 20 pills three times per day) or standard treatment group (10 pills CDDP and 10 pills placebo three times per day). Patients will have a 6-week medication period and be followed up every 2 weeks. The primary endpoint is the change of total exercise time from baseline to week 6 as assessed by cardiopulmonary exercise testing (CPET). Secondary endpoints include changes in the frequency of angina, Canadian Cardiovascular Society angina class, nitroglycerin use, Seattle Angina Questionnaire scores, peak oxygen uptake (VO(2) peak) and other parameters as measured by CPET, and the levels of plasma C-reactive protein, homocysteine, and N-terminal pro-B-type natriuretic peptide. Safety events related to CDDP use will be monitored. ETHICS AND DISSEMINATION: The research had been approved by the Clinical research and laboratory animal ethics committee of the First Affiliated Hospital, Sun Yat-sen University ([2019]65). The results will be reported through peer-reviewed journals, seminars, and conference presentations. TRIAL REGISTRATION NUMBER: www.chictr.org.cn (ChiCTR2000032384). Registered on 27 April 2020.
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spelling pubmed-90887382022-05-11 Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial Wu, Zexuan Xu, Danping Wu, Zhen Chen, Ailan Liu, Lijuan Ling, Li Zhou, Yan Liu, Duoduo Liu, Yin Dong, Yugang Chen, Yili Front Cardiovasc Med Cardiovascular Medicine INTRODUCTION: Patients with incomplete revascularization (ICR) tend to develop refractory angina despite optimal medical therapy. The Compound Danshen Dripping Pills (CDDP) is a widely used antianginal drug in China and is shown to significantly alleviate myocardial ischemia. Previous studies showed dose-efficacy tendency when increasing doses of CDDP. This study aims to investigate the efficacy and safety of intensive doses of CDDP in patients with refractory angina with ICR. METHODS AND ANALYSIS: The INCODER study is a multicenter, double-blind, randomized controlled, superiority trial. We plan to recruit 250 patients aged 18–85 years with a diagnosis of refractory angina with ICR. Patients will be randomized (1:1) to intensive treatment group (CDDP 20 pills three times per day) or standard treatment group (10 pills CDDP and 10 pills placebo three times per day). Patients will have a 6-week medication period and be followed up every 2 weeks. The primary endpoint is the change of total exercise time from baseline to week 6 as assessed by cardiopulmonary exercise testing (CPET). Secondary endpoints include changes in the frequency of angina, Canadian Cardiovascular Society angina class, nitroglycerin use, Seattle Angina Questionnaire scores, peak oxygen uptake (VO(2) peak) and other parameters as measured by CPET, and the levels of plasma C-reactive protein, homocysteine, and N-terminal pro-B-type natriuretic peptide. Safety events related to CDDP use will be monitored. ETHICS AND DISSEMINATION: The research had been approved by the Clinical research and laboratory animal ethics committee of the First Affiliated Hospital, Sun Yat-sen University ([2019]65). The results will be reported through peer-reviewed journals, seminars, and conference presentations. TRIAL REGISTRATION NUMBER: www.chictr.org.cn (ChiCTR2000032384). Registered on 27 April 2020. Frontiers Media S.A. 2022-04-26 /pmc/articles/PMC9088738/ /pubmed/35557513 http://dx.doi.org/10.3389/fcvm.2022.860059 Text en Copyright © 2022 Wu, Xu, Wu, Chen, Liu, Ling, Zhou, Liu, Liu, Dong and Chen. 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 Cardiovascular Medicine
Wu, Zexuan
Xu, Danping
Wu, Zhen
Chen, Ailan
Liu, Lijuan
Ling, Li
Zhou, Yan
Liu, Duoduo
Liu, Yin
Dong, Yugang
Chen, Yili
Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial
title Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial
title_full Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial
title_fullStr Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial
title_full_unstemmed Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial
title_short Efficacy of INtensive Treatment vs. Standard Treatment of COmpound DanshEn Dripping Pills in Refractory Angina Patients With Incomplete Revascularization (INCODER Study): Study Protocol for a Multicenter, Double-Blind, Randomized Controlled, Superiority Trial
title_sort efficacy of intensive treatment vs. standard treatment of compound danshen dripping pills in refractory angina patients with incomplete revascularization (incoder study): study protocol for a multicenter, double-blind, randomized controlled, superiority trial
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088738/
https://www.ncbi.nlm.nih.gov/pubmed/35557513
http://dx.doi.org/10.3389/fcvm.2022.860059
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