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Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial

BACKGROUND: No treatment has convincingly been proven to be beneficial for microvascular obstruction (MVO) in patients with ST-elevation myocardial infarction (STEMI). Several studies have described the effects of Danhong Injection. However, evidence of a rigorously designed verification study is st...

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Autores principales: Zhang, Xiaoyu, Tian, Guihua, Shi, Zhaofeng, Sun, Yang, Hu, Jiayuan, Jiang, Yin, Zheng, Rui, Chen, Shiqi, Li, Chengyu, Yang, Xinyu, He, Tianmai, Han, Songjie, Zhang, Chi, Zhang, Lijing, Liu, Yan, Shang, Hongcai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950857/
https://www.ncbi.nlm.nih.gov/pubmed/31915046
http://dx.doi.org/10.1186/s13063-019-3947-6
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author Zhang, Xiaoyu
Tian, Guihua
Shi, Zhaofeng
Sun, Yang
Hu, Jiayuan
Jiang, Yin
Zheng, Rui
Chen, Shiqi
Li, Chengyu
Yang, Xinyu
He, Tianmai
Han, Songjie
Zhang, Chi
Zhang, Lijing
Liu, Yan
Shang, Hongcai
author_facet Zhang, Xiaoyu
Tian, Guihua
Shi, Zhaofeng
Sun, Yang
Hu, Jiayuan
Jiang, Yin
Zheng, Rui
Chen, Shiqi
Li, Chengyu
Yang, Xinyu
He, Tianmai
Han, Songjie
Zhang, Chi
Zhang, Lijing
Liu, Yan
Shang, Hongcai
author_sort Zhang, Xiaoyu
collection PubMed
description BACKGROUND: No treatment has convincingly been proven to be beneficial for microvascular obstruction (MVO) in patients with ST-elevation myocardial infarction (STEMI). Several studies have described the effects of Danhong Injection. However, evidence of a rigorously designed verification study is still lacking, and the intervention timing of Danhong Injection is uncertain. METHODS: The DIRECTION study is a multicenter, prospective, randomized, evaluator-blind study. A total of 336 patients with STEMI receiving percutaneous coronary intervention (PCI) will be randomly assigned to conventional treatment, the preoperative Danhong Injection, or the postoperative Danhong Injection. The primary outcome is rate of ST-segment resolution (STR) ≥ 70% at 90 min after PCI. The secondary outcomes are the degree of STR, Thrombolysis in Myocardial Infarction (TIMI) flow grade, TIMI myocardial perfusion grade, left ventricular ejection fraction, N-terminal prohormone brain natriuretic peptide, high-sensitivity C-reactive protein, and infarct size expressed as area under the curve for cardiac troponin I (cTnI) and for creatine kinase MB. The major adverse cardiovascular events and hospital readmission events will be recorded. Health quality will be assessed with the 12-item Short Form Health Survey. The safety outcomes include bleeding events, adverse events, and abnormal changes in routine blood tests. Psychological status and dietary patterns will be evaluated using Hamilton Depression Rating Scale and Food Frequency Questionnaire as the relevant indicators. DISCUSSION: This trial will evaluate the efficacy and safety of Danhong Injection, as well as its optimal timing of intervention to prevent MVO in patients with STEMI. TRIAL REGISTRATION: Chinese Clinical Trial Registry, ChiCTR1900021440. Registered on February 21, 2019.
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spelling pubmed-69508572020-01-09 Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial Zhang, Xiaoyu Tian, Guihua Shi, Zhaofeng Sun, Yang Hu, Jiayuan Jiang, Yin Zheng, Rui Chen, Shiqi Li, Chengyu Yang, Xinyu He, Tianmai Han, Songjie Zhang, Chi Zhang, Lijing Liu, Yan Shang, Hongcai Trials Study Protocol BACKGROUND: No treatment has convincingly been proven to be beneficial for microvascular obstruction (MVO) in patients with ST-elevation myocardial infarction (STEMI). Several studies have described the effects of Danhong Injection. However, evidence of a rigorously designed verification study is still lacking, and the intervention timing of Danhong Injection is uncertain. METHODS: The DIRECTION study is a multicenter, prospective, randomized, evaluator-blind study. A total of 336 patients with STEMI receiving percutaneous coronary intervention (PCI) will be randomly assigned to conventional treatment, the preoperative Danhong Injection, or the postoperative Danhong Injection. The primary outcome is rate of ST-segment resolution (STR) ≥ 70% at 90 min after PCI. The secondary outcomes are the degree of STR, Thrombolysis in Myocardial Infarction (TIMI) flow grade, TIMI myocardial perfusion grade, left ventricular ejection fraction, N-terminal prohormone brain natriuretic peptide, high-sensitivity C-reactive protein, and infarct size expressed as area under the curve for cardiac troponin I (cTnI) and for creatine kinase MB. The major adverse cardiovascular events and hospital readmission events will be recorded. Health quality will be assessed with the 12-item Short Form Health Survey. The safety outcomes include bleeding events, adverse events, and abnormal changes in routine blood tests. Psychological status and dietary patterns will be evaluated using Hamilton Depression Rating Scale and Food Frequency Questionnaire as the relevant indicators. DISCUSSION: This trial will evaluate the efficacy and safety of Danhong Injection, as well as its optimal timing of intervention to prevent MVO in patients with STEMI. TRIAL REGISTRATION: Chinese Clinical Trial Registry, ChiCTR1900021440. Registered on February 21, 2019. BioMed Central 2020-01-08 /pmc/articles/PMC6950857/ /pubmed/31915046 http://dx.doi.org/10.1186/s13063-019-3947-6 Text en © The Author(s). 2020 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
Zhang, Xiaoyu
Tian, Guihua
Shi, Zhaofeng
Sun, Yang
Hu, Jiayuan
Jiang, Yin
Zheng, Rui
Chen, Shiqi
Li, Chengyu
Yang, Xinyu
He, Tianmai
Han, Songjie
Zhang, Chi
Zhang, Lijing
Liu, Yan
Shang, Hongcai
Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial
title Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial
title_full Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial
title_fullStr Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial
title_full_unstemmed Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial
title_short Initiate Danhong Injection before or after percutaneous coronary intervention for microvascular obstruction in ST-elevation myocardial infarction (DIRECTION): study protocol for a randomized controlled trial
title_sort initiate danhong injection before or after percutaneous coronary intervention for microvascular obstruction in st-elevation myocardial infarction (direction): study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950857/
https://www.ncbi.nlm.nih.gov/pubmed/31915046
http://dx.doi.org/10.1186/s13063-019-3947-6
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