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Abstract

Background

Co-morbid hypertension is strong predictor of adverse cardiovascular (CV) outcomes in patients with atrial fibrillation (AF) but the optimal target for blood pressure (BP) control in this patient population has not been clearly defined.

Methods

The Cardiovascular Risk reduction in patients with Atrial Fibrillation Trial (CRAFT) is an investigator-initiated and conducted, international, multicenter, open-label, parallel-group, blinded outcome assessed, randomized controlled trial of intensive BP control in patients with AF. The aim is to determine whether intensive BP control (target home systolic blood pressure [SBP] <120 mmHg) is superior to standard BP control (home SBP <135 mmHg) on the hierarchical composite outcome of time to CV death, number of stroke events, time to the first stroke, number of myocardial infarction (MI) events, time to the first MI, number of heart failure hospitalization (HFH) events, and time to the first HFH. A sample size of 1,675 patients is estimated to provide 80% power to detect a win-ratio of 1.50 for intensive versus standard BP control on the primary composite outcome. Study visits are conducted at 1, 2, 3, and 6 months postrandomization, and every 6 months thereafter during the study.

Conclusions

This clinical trial aims to provide reliable evidence of the effects of intensive BP control in patients with AF.

Trial registration

The trial is registered at ClinicalTrials.gov (NCT04347330)

Details

Title
Protocol for a randomized controlled trial of intensive blood pressure control on cardiovascular risk reduction in patients with atrial fibrillation: Rationale and design of the CRAFT trial
Author
Jiang, Chao 1 ; Wang, Zhiyan 2 ; Du, Xin 1 ; Wang, Yufeng 2 ; Gao, Mingyang 2 ; Jia, Zhaoxu 2 ; Chai, Zhongyi 3 ; Yang, Zhiyun 4 ; Wang, Chi 5 ; Liu, He 2 ; Hu, Rong 2 ; Lv, Qiang 2 ; Wu, Jiahui 2 ; Xu, Li 2 ; Jia, Changqi 2 ; Han, Rong 5 ; Arima, Hisatomi 6 ; Wang, Xia 7 ; Neal, Bruce 8 ; Rodgers, Anthony 7 ; Hillis, Graham S 9 ; Patel, Anushka 7 ; Li, Qiang 7 ; Dong, Jianzeng 1 ; Anderson, Craig S 10 ; Ma, Changsheng 2 

 Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China; National Clinical Research Center for Cardiovascular Diseases, Beijing, China; Heart Health Research Center, Beijing, China 
 Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China; National Clinical Research Center for Cardiovascular Diseases, Beijing, China 
 Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Henan Province, China 
 Department of Cardiology, Peking University Third Hospital, Beijing, China 
 Heart Health Research Center, Beijing, China 
 Department of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan 
 The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, Australia 
 The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, Australia; School of Public Health, Imperial College London, London, UK 
 Department of Cardiology, Royal Perth Hospital and Medical School, University of Western Australia, Perth, Western Australia, Australia 
10  Heart Health Research Center, Beijing, China; The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, Australia; Department of Neurology, Royal Prince Alfred Hospital, University of Sydney, Sydney, Australia; Institute for Science and Techology for Brain-inspired Intelligence, Fudan University, Shanghai, China 
Publication title
Volume
278
Pages
33-40
Publication year
2024
Publication date
Dec 2024
Section
Study Protocol
Publisher
Elsevier Limited
Place of publication
Philadelphia
Country of publication
United Kingdom
ISSN
00028703
e-ISSN
10976744
Source type
Scholarly Journal
Language of publication
English
Document type
Evidence Based Healthcare, Journal Article
ProQuest document ID
3126500831
Document URL
https://www.proquest.com/scholarly-journals/protocol-randomized-controlled-trial-intensive/docview/3126500831/se-2?accountid=208611
Copyright
Copyright Elsevier Limited Dec 2024
Last updated
2024-11-14