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Rationale and design of EXPLORE: a randomized, prospective, multicenter trial investigating the impact of recanalization of a chronic total occlusion on left ventricular function in patients after primary percutaneous coronary intervention for acute ST-elevation myocardial infarction

Authors :
van der Schaaf, Rene J.
Claessen, Bimmer E.
Hoebers, Loes P.
Verouden, Niels J.
Koolen, Jacques J.
Suttorp, Maarten J.
Barbato, Emanuele
Bax, Matthijs
Strauss, Bradley H.
Olivecrona, Goran K.
Tuseth, Vegard
Glogar, Dietmar
Ramunddal, Truls
Tijssen, Jan G.
Piek, Jan J.
Henriques, Jose P.
Investigators, Explore
Faculteit der Geneeskunde
Cardiology
ACS - Amsterdam Cardiovascular Sciences
Graduate School
van der Schaaf, R. J.
Claessen, B. E.
Hoebers, L. P.
Verouden, N. J.
Koolen, J. J.
Suttorp, M. J.
Barbato, Emanuele
Bax, M.
Strauss, B. H.
Olivecrona, G. K.
Tuseth, V.
Glogar, D. j.
RÃ¥munddal, T.
Tijssen, J. G.
Piek, J. J.
Henriques, J. P. S.
Source :
Trials; 11 (2010), Trials, 11:89. BioMed Central, Trials, Trials, Vol 11, Iss 1, p 89 (2010), Trials, 11(1). BioMed Central
Publication Year :
2010
Publisher :
BioMed Central (BMC), 2010.

Abstract

Background In the setting of primary percutaneous coronary intervention, patients with a chronic total occlusion in a non-infarct related artery were recently identified as a high-risk subgroup. It is unclear whether ST-elevation myocardial infarction patients with a chronic total occlusion in a non-infarct related artery should undergo additional percutaneous coronary intervention of the chronic total occlusion on top of optimal medical therapy shortly after primary percutaneous coronary intervention. Possible beneficial effects include reduction in adverse left ventricular remodeling and preservation of global left ventricular function and improved clinical outcome during future coronary events. Methods/Design The Evaluating Xience V and left ventricular function in Percutaneous coronary intervention on occLusiOns afteR ST-Elevation myocardial infarction (EXPLORE) trial is a randomized, prospective, multicenter, two-arm trial with blinded evaluation of endpoints. Three hundred patients after primary percutaneous coronary intervention for ST-elevation myocardial infarction with a chronic total occlusion in a non-infarct related artery are randomized to either elective percutaneous coronary intervention of the chronic total occlusion within seven days or standard medical treatment. When assigned to the invasive arm, an everolimus-eluting coronary stent is used. Primary endpoints are left ventricular ejection fraction and left ventricular end-diastolic volume assessed by cardiac Magnetic Resonance Imaging at four months. Clinical follow-up will continue until five years. Discussion The ongoing EXPLORE trial is the first randomized clinical trial powered to investigate whether recanalization of a chronic total occlusion in a non-infarct related artery after primary percutaneous coronary intervention for ST-elevation myocardial infarction results in a better preserved residual left ventricular ejection fraction, reduced end-diastolic volume and enhanced clinical outcome. Trial registration trialregister.nl NTR1108.

Subjects

Subjects :
medicine.medical_treatment
Left
Myocardial Infarction
recanalization
Study Protocol
Clinical Protocols
heart contraction
dipeptidyl carboxypeptidase inhibitor
Drug-Eluting Stent
acetylsalicylic acid
antilipemic agent
beta adrenergic receptor blocking agent
clopidogrel
everolimus
prasugrel
cardiovascular agent
drug derivative
rapamycin
acute disease
artery occlusion
article
chronic total occlusion
clinical research
clinical trial
controlled clinical trial
controlled study
follow up
heart left ventricle enddiastolic volume
heart left ventricle function
heart ventricle remodeling
human
major clinical study
methodology
multicenter study
nuclear magnetic resonance imaging
percutaneous coronary intervention
randomized controlled trial
ST segment elevation myocardial infarction
Canada
chronic disease
clinical protocol
convalescence
drug eluting stent
Europe
heart infarction
heart stroke volume
instrumentation
pathophysiology
prospective study
prosthesis
time
transluminal coronary angioplasty
treatment outcome
Angioplasty
Balloon
Coronary
Cardiovascular Agents
Chronic Disease
Coronary Occlusion
Drug-Eluting Stents
Humans
Magnetic Resonance Imaging
Myocardial Contraction
Ontario
Prospective Studies
Prosthesis Design
Recovery of Function
Research Design
Sirolimus
Stroke Volume
Time Factors
Treatment Outcome
Ventricular Function
Sirolimu
Pharmacology (medical)
Cardiac and Cardiovascular Systems
Myocardial infarction
Angioplasty, Balloon, Coronary
treatment outcome, Angioplasty, Balloon, Coronary
cardiovascular system
lcsh:Medicine (General)
medicine.medical_specialty
Multicenter trial
Everolimus
medicine.disease
Prospective Studie
Myocardial infarction complications
rapamycin, acute disease
Medicine (miscellaneous)
Ventricular Function, Left
lcsh:R5-920
prosthesi
Cardiology
Time Factor
Internal medicine
Coronary stent
medicine
cardiovascular diseases
Ventricular remodeling
business.industry
everolimu
Percutaneous coronary intervention
Surgery
Coronary occlusion
business

Details

Language :
English
ISSN :
17456215
Database :
OpenAIRE
Journal :
Trials; 11 (2010), Trials, 11:89. BioMed Central, Trials, Trials, Vol 11, Iss 1, p 89 (2010), Trials, 11(1). BioMed Central
Accession number :
edsair.doi.dedup.....cc9838c410ec93d9f4909d7abf2ff7e2