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RECRUITINGOBSERVATIONAL

SUPRAFLEX CRUZ PMCF Study ( rEpic05 )

SUPRAFLEX CRUZPost-Market Clinical Follow-up Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Multicenter, prospective, non-randomized, post-market clinical follow-up (PMCF) study to confirm and support the clinical safety and performance of Medical Device Regulations (MDR) with multivessel coronary disease requirements in all the CONSECUTIVE patients treated with (SUPRAFLEX CRUZ).

Who May Be Eligible (Plain English)

Who May Qualify: - ≥ 18 years old and; - Patients treated with SUPRAFLEX CRUZ according to routine hospital practice and following instructions for use - Patients with multivessel coronary artery disease (understood as that which affects more than one territory of the major epicardial coronary arteries - anterior descending, circumflex, right coronary artery) who is treated with more than 1 stent under study in lesions located in more than 1 of the aforementioned arteries. - Substudy: Patients with Ejection Fraction \<45% by Echocardiography - willing to sign a consent form signed Who Should NOT Join This Trial: - Not meet inclusion criteria - Contraindication for antiplatelet treatment - Patient life expectancy less than 12 months Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * ≥ 18 years old and; * Patients treated with SUPRAFLEX CRUZ according to routine hospital practice and following instructions for use * Patients with multivessel coronary artery disease (understood as that which affects more than one territory of the major epicardial coronary arteries - anterior descending, circumflex, right coronary artery) who is treated with more than 1 stent under study in lesions located in more than 1 of the aforementioned arteries. * Substudy: Patients with Ejection Fraction \<45% by Echocardiography * Informed consent signed Exclusion Criteria: * Not meet inclusion criteria * Contraindication for antiplatelet treatment * Patient life expectancy less than 12 months

Treatments Being Tested

DEVICE

SUPRAFLEX CRUZ

Patients in whom treatment with SUPRAFLEX CRUZ has been attempted

Locations (20)

Hospital General Universitario de Elche
Elche, Alicante, Spain
Hospital Universitario A Coruña
A Coruña, Spain
Hospital Universitario de Cruces
Barakaldo, Spain
Hospital Universitari Vall D'Hebron
Barcelona, Spain
Hospital de La Santa Creu I Sant Pau
Barcelona, Spain
Hospital General Universitario de Castellón
Castelló, Spain
Hospital Universitario San Pedro de Alcántara
Cáceres, Spain
Hospital General Universitario de Ciudad Real
Ciudad Real, Spain
Hospital Universitari Dr. Josep Trueta
Girona, Spain
Hospital Universitario Clínico San Cecilio
Granada, Spain
Hospital Universitario de Leon
León, Spain
Hospital Universitari Arnau de Vilanova
Lleida, Spain
Hospital Universitario 12 de Octubre
Madrid, Spain
Hospital Clínico Universitario Virgen de la Arrixaca
Murcia, Spain
Hospital Parc Tauli
Sabadell, Spain
Hospital Clinico Universitario de Salamanca
Salamanca, Spain
Hospital Clínico Universitario de Santiago de Compostela
Santiago de Compostela, Spain
Hospital Universitario Virgen Del Rocio
Seville, Spain
Hospital Universitario de Toledo
Toledo, Spain
Hospital Universitario Y Politécnico La Fé
Valencia, Spain