Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/174448
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dc.contributor.authorChaccour, Carlos-
dc.contributor.authorRuiz Castillo, Paula-
dc.contributor.authorRichardson, Mary-Ann-
dc.contributor.authorMoncunill, Gemma-
dc.contributor.authorCasellas, Aina-
dc.contributor.authorCarmona Torre, Francisco-
dc.contributor.authorGiráldez, Miriam-
dc.contributor.authorSchwartz Mota, Juana-
dc.contributor.authorYuste, José R.-
dc.contributor.authorAzanza, José Ramón-
dc.contributor.authorFernández, Miriam-
dc.contributor.authorReina, Gabriel-
dc.contributor.authorDobaño, Carlota, 1969--
dc.contributor.authorBrew, Joe-
dc.contributor.authorSadaba, Belen-
dc.contributor.authorHammann, Felix-
dc.contributor.authorRabinovich, Regina-
dc.date.accessioned2021-03-01T07:28:48Z-
dc.date.available2021-03-01T07:28:48Z-
dc.date.issued2020-06-08-
dc.identifier.issn1745-6215-
dc.identifier.urihttp://hdl.handle.net/2445/174448-
dc.description.abstractObjectives: The primary objective is to determine the efficacy of a single dose of ivermectin, administered to low risk, non-severe COVID-19 patients in the first 48 hours after symptom onset to reduce the proportion of patients with detectable SARS-CoV-2 RNA by Polymerase Chain Reaction (PCR) test from nasopharyngeal swab at day 7 post-treatment.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherBioMed Central-
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1186/s13063-020-04421-z-
dc.relation.ispartofTrials, 2020, vol. 21-
dc.relation.urihttp://dx.doi.org/10.1186/s13063-020-04421-z-
dc.rightscc by (c) Chaccour et al., 2020-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (ISGlobal)-
dc.subject.classificationSARS-CoV-2-
dc.subject.classificationMedicaments antivírics-
dc.subject.otherSARS-CoV-2-
dc.subject.otherAntiviral agents-
dc.titleThe SARS-CoV-2 Ivermectin Navarra-ISGlobal Trial (SAINT) to Evaluate the Potential of Ivermectin to Reduce COVID-19 Transmission in low risk, non-severe COVID-19 patients in the first 48 hours after symptoms onset: A structured summary of a study protocol for a randomized control pilot trial-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2021-02-26T19:00:57Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid32513289-
Appears in Collections:Articles publicats en revistes (ISGlobal)

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