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dc.contributor.authorReveiz, Ludovic
dc.contributor.authorChan, An-Wen
dc.contributor.authorKrleza-Jeric, Karmela
dc.contributor.authorGranados, Carlos Eduardo
dc.contributor.authorPinart, Mariona
dc.contributor.authorEtxeandia, Itziar
dc.contributor.authorRada, Diego
dc.contributor.authorMartínez Alonso, Montserrat
dc.contributor.authorBonfill, Xavier
dc.contributor.authorCardona, Andrés Felipe
dc.date.accessioned2011-10-31T10:13:12Z
dc.date.available2011-10-31T10:13:12Z
dc.date.issued2010
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10459.1/41667
dc.description.abstractBackground: Although randomized clinical trials (RCTs) are considered the gold standard of evidence, their reporting is often suboptimal. Trial registries have the potential to contribute important methodologic information for critical appraisal of study results. Methods and Findings: The objective of the study was to evaluate the reporting of key methodologic study characteristics in trial registries. We identified a random sample (n = 265) of actively recruiting RCTs using the World Health Organization International Clinical Trials Registry Platform (ICTRP) search portal in 2008. We assessed the reporting of relevant domains from the Cochrane Collaboration’s ‘Risk of bias’ tool and other key methodological aspects. Our primary outcomes were the proportion of registry records with adequate reporting of random sequence generation, allocation concealment, blinding, and trial outcomes. Two reviewers independently assessed each record. Weighted overall proportions in the ICTRP search portal for adequate reporting of sequence generation, allocation concealment, blinding (including and excluding open label RCT) and primary outcomes were 5.7% (95% CI 3.0–8.4%), 1.4% (0–2.8%), 41% (35–47%), 8.4% (4.1–13%), and 66% (60–72%), respectively. The proportion of adequately reported RCTs was higher for registries that used specific methodological fields for describing methods of randomization and allocation concealment compared to registries that did not. Concerning other key methodological aspects, weighted overall proportions of RCTs with adequately reported items were as follows: eligibility criteria (81%), secondary outcomes (46%), harm (5%) follow-up duration (62%), description of the interventions (53%) and sample size calculation (1%). Conclusions: Trial registries currently contain limited methodologic information about registered RCTs. In order to permit adequate critical appraisal of trial results reported in journals and registries, trial registries should consider requesting details on key RCT methods to complement journal publications. Full protocols remain the most comprehensive source of methodologic information and should be made publicly available.ca_ES
dc.language.isoengca_ES
dc.publisherPublic Library of Science (PLoS)ca_ES
dc.relation.isformatofReproducció del document publicat a https://doi.org/10.1371%2Fjournal.pone.0012484ca_ES
dc.relation.ispartofPLoS ONE, 2010, vol. 5, núm. 8, e12484ca_ES
dc.rightscc-by, (c) Reveiz et al., 2010ca_ES
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/es/deed.caca_ES
dc.subject.otherAssaigs clínicsca_ES
dc.subject.otherMedicina basada en l'evidènciaca_ES
dc.subject.otherAssaigs clínics -- Bases de dadesca_ES
dc.titleReporting of methodologic information on trial registries for quality assessment: a study of trial records retrieved from the WHO search portalca_ES
dc.typearticleca_ES
dc.identifier.idgrec016421
dc.type.versionpublishedVersionca_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.identifier.doihttps://doi.org/10.1371%2Fjournal.pone.0012484


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cc-by, (c) Reveiz et al., 2010
Except where otherwise noted, this item's license is described as cc-by, (c) Reveiz et al., 2010