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dc.contributor.authorDávila Fajardo, Cristina Lucía
dc.contributor.authorSánchez Ramos, Jesús Gabriel
dc.contributor.authorDíaz Villamarín, Xando 
dc.contributor.authorMartínez González, Luis Javier 
dc.contributor.authorToledo Frías, Pablo
dc.contributor.authorMartínez Huertas, Susana
dc.contributor.authorBurillo Gómez, Francisco
dc.contributor.authorCaballero Borrego, Juan
dc.contributor.authorBautista Pavés, Alicia
dc.contributor.authorMarín Guzmán, María Carmen
dc.contributor.authorRamírez Hernández, José Antonio 
dc.contributor.authorCorrea Vilches, Concepción
dc.contributor.authorCabeza Barrera, José
dc.date.accessioned2021-02-05T12:10:07Z
dc.date.available2021-02-05T12:10:07Z
dc.date.issued2016-12-20
dc.identifier.citationC. L. Dávila-Fajardo et al. The study protocol for a non-randomized controlled clinical trial using a genotype-guided strategy in a dataset of patients who undergone percutaneous coronary intervention with stent. Data in Brief 10 (2017) 518–524 [https://doi.org/10.1016/j.dib.2016.12.019]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/66329
dc.description.abstractThis article contains data related to the research article entitled “Results of genotype–guided antiplatelet therapy in patients undergone percutaneous coronary intervention with stent” (J. Sánchez-Ramos, C.L. Dávila-Fajardo, P. Toledo Frías, X. Díaz Villamarín, L.J. Martínez-González, S. Martínez Huertas, F. Burillo Gómez, J. Caballero Borrego, A. Bautista Pavés, M.C. Marín Guzmán, J.A. Ramirez Hernández, C. Correa Vilches, J. Cabeza Barrera, 2016) (1). This data article reports, for the first time, about the non-randomized clinical trial protocol that check if CYP2C19/ABCB1 genotype–guided strategy in which the choice of antiplatelet therapy is based on the genetic test, reduces the rates of cardiovascular events and bleeding compared to a non-tailored strategy in patients undergone percutaneous coronary intervention (PCI) with stent. The data included in this article are: design and setting of the study, study population, inclusion and exclusion criteria, definition of the intervention, objectives, variables (baseline characteristics and during the follow-up), study procedures, collection and treatment of the biological sample, genotyping, withdrawal criteria, sample size, statistic analysis, ethical aspects, information sheet and consent form. The authors confirm that this study has been registered in Eudra CT (Eudra CT: 2016-001294-33).es_ES
dc.description.sponsorshipMinistry of Health of Government of Andalusia PI-057/2012es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectClinical trial protocoles_ES
dc.titleThe study protocol for a non-randomized controlled clinical trial using a genotype-guided strategy in a dataset of patients who undergone percutaneous coronary intervention with stentes_ES
dc.typedatasetes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1016/j.dib.2016.12.019
dc.identifier.doi10.30827/Digibug.66329
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.publication.year2016


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