Study protocol for a randomised controlled trial: harmonising optimal strategy for treatment of coronary artery stenosis - coronary intervention with next-generation drug-eluting stent platforms and abbreviated dual antiplatelet therapy (HOST-IDEA) trial

被引:8
作者
Kim, Chi-Hoon [1 ,2 ]
Han, Jung-Kyu [1 ,2 ]
Yang, Han-Mo [1 ,2 ]
Park, Kyung Woo [1 ,2 ]
Lee, Hae-Young [1 ,2 ]
Kang, Hyun-Jae [1 ,2 ]
Koo, Bon-Kwon [1 ,2 ]
Lee, Namho [3 ,4 ]
Cha, Tae-Joon [5 ,6 ]
Yang, Tae-Hyun [7 ,8 ]
Jeong, Myung-Ho [9 ,10 ]
Yoon, Myeong-Ho [11 ,12 ]
Lee, Seung Uk [13 ]
Lee, Seung Jin [14 ,15 ]
Kim, Jin Won [16 ,17 ]
Cho, Jin-Man [18 ,19 ]
Han, Kyu-Rock [20 ,21 ]
Pyun, Wook Bum [22 ,23 ]
Kim, Hyo-Soo [1 ,2 ]
机构
[1] Seoul Natl Univ Hosp, Cardiovasc Ctr, Dept Internal Med, Seoul, South Korea
[2] Seoul Natl Univ Hosp, Div Cardiol, Seoul, South Korea
[3] Hallym Univ, Kangnam Sacred Heart Hosp, Dept Internal Med, Seoul, South Korea
[4] Hallym Univ, Kangnam Sacred Heart Hosp, Div Cardiol, Seoul, South Korea
[5] Kosin Univ, Gospel Hosp, Dept Internal Med, Busan, South Korea
[6] Kosin Univ, Gospel Hosp, Div Cardiol, Busan, South Korea
[7] Inje Univ, Busan Paik Hosp, Dept Internal Med, Busan, South Korea
[8] Inje Univ, Busan Paik Hosp, Div Cardiol, Busan, South Korea
[9] Chonnam Natl Univ Hosp, Dept Internal Med, Gwangju, South Korea
[10] Chonnam Natl Univ Hosp, Div Cardiol, Gwangju, South Korea
[11] Ajou Univ Hosp, Dept Internal Med, Suwon, South Korea
[12] Ajou Univ Hosp, Div Cardiol, Suwon, South Korea
[13] Kwangju Christian Hosp, Cardiovasc Ctr, Gwangju, South Korea
[14] Soon Chun Hyang Univ, Cheonan Hosp, Dept Internal Med, Cheonan, South Korea
[15] Soon Chun Hyang Univ, Cheonan Hosp, Div Cardiol, Cheonan, South Korea
[16] Korea Univ, Guro Hosp, Dept Internal Med, Seoul, South Korea
[17] Korea Univ, Guro Hosp, Div Cardiol, Seoul, South Korea
[18] Kyung Hee Univ Hosp Gangdong, Dept Internal Med, Seoul, South Korea
[19] Kyung Hee Univ Hosp Gangdong, Div Cardiol, Seoul, South Korea
[20] Hallym Univ, Kangdong Sacred Hosp, Dept Internal Med, Seoul, South Korea
[21] Hallym Univ, Kangdong Sacred Hosp, Div Cardiol, Seoul, South Korea
[22] Ewha Womans Univ, Mokdong Hosp, Med Ctr, Dept Internal Med, Seoul, South Korea
[23] Ewha Womans Univ, Mokdong Hosp, Med Ctr, Div Cardiol, Seoul, South Korea
关键词
ASSOCIATION TASK-FORCE; AMERICAN-COLLEGE; CLINICAL-TRIALS; FOLLOW-UP; DURATION; EFFICACY; IMPLANTATION; DEFINITIONS; GUIDELINE; DISEASE;
D O I
10.1136/bmjopen-2017-016617
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction We have recently seen the introduction of newer generation drug-eluting stents with ultrathin struts that use advanced polymer technologies. However, the efficacy and safety of these newest stents have not yet been fully explored. In addition, there are still controversies over the optimal duration of dual antiplatelet therapy (DAPT) after stent implantation, particularly for ultrathin stents with the newest polymer technologies. Methods and analysis The HOST-IDEA trial is a randomised, open-label, multicentre, non-inferiority trial and the first study to directly compare two of these ultrathin sirolimus-eluting stents: Orsiro stent with biodegradable polymer, and polymerfree Coroflex ISAR (CX-ISAR) stent. This study has a scheme of 2x2 factorial design according to the stent type and DAPT duration (3 vs 12 months). A total of 2152 patients will be randomised and stratified to demonstrate the non-inferiority of CXISAR to Orsiro, or of the abbreviated DAPT duration to the conventional 12 months (both in 1: 1 ratio). For the comparison of stent type, the primary endpoint is target lesion failure (TLF), which is a composite of cardiac death, target vessel-related myocardial infarction and clinically driven target lesion revascularisation. For the comparison of DAPT duration, the net adverse clinical event is the coprimary endpoint, which is defined as a composite of TLF, definite/probable stent thrombosis and major bleeding. Ethic approval and dissemination All the institutions involved in this study are required to have ethical approval prior to patient enrolment. This multicentre study will recruit patients through competitive registration, but institutions that have not yet obtained ethical approvals have made it impossible to enrol patients in a centralised web database. The final results will be presented at relevant international conferences and will be materialised in the form of papers.
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页数:8
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