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Consistency of trial reporting between ClinicalTrials.gov and corresponding publications: one decade after FDAAA

The FDA Amendments Act (FDAAA) required that information for certain clinical trials, such as details about study design features and endpoints, as well as results, be publicly reported in ClinicalTrials.gov. We conducted a cross-sectional analysis of phase III trials with primary results published...

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Bibliografische gegevens
Gepubliceerd in:Trials
Hoofdauteurs: Talebi, Ramtin, Redberg, Rita F., Ross, Joseph S.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2020
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7376878/
https://ncbi.nlm.nih.gov/pubmed/32703252
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13063-020-04603-9
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