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Nordic trial reporting project: Raw data from EU Clinical Trials Registry (EUCTR) and ClinicalTrials.gov

This dataset contains raw data from EUCTR and ClinicalTrials.gov, used to evaluate clinical trial reporting at medical universities and university hospitals in the Nordic countries.

AccessFree to access
LicenceLicense statement is still being checked
Producerauthor team for the research project "Systematic evaluation of clinical trial reporting at medical universities and university hospitals in the Nordic countries"

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Public health & medicineFree to access

Key facts

Institutionauthor team for the research project "Systematic evaluation of clinical trial reporting at medical universities and university hospitals in the Nordic countries"
CoverageNordic countries (Denmark, Finland, Iceland, Norway, Sweden) medical universities and university hospitals
Time spanEUCTR data as of Nov 7, 2022; ClinicalTrials.gov data as of Nov 9, 2022
Scale3 files

Contents & fields

This dataset contains raw data from EUCTR and ClinicalTrials.gov, including the EU Trials Tracker dataset for EUCTR trials, custom web scraper data from EUCTR country protocols and results sections (variables described in Appendix Table 2), and the complete AACT dataset from ClinicalTrials.gov. The dataset consists of 3 files.

  • EUCTR trials tracker dataset——Dataset of EUCTR trials from the EU Trials Tracker
  • Custom web scraper data——Data extracted from EUCTR country protocols and results sections (variables in Appendix Table 2)
  • AACT dataset——Complete Aggregate Analysis of ClinicalTrials.gov dataset

Research uses

Can be used to assess compliance of clinical trial reporting in Nordic countries, analyze delays in result reporting, etc.

Information comes from the source page. Please check that page for current details and terms.

Keywords

clinical trialsreportingNordicEUCTRClinicalTrials.govraw data

Access and licence

Licence: License statement is still being checked | Free to access

Official site / download →

Why this is hard to get on your own

When obtaining raw data on Nordic clinical trial reporting, one often needs to integrate multiple registries with inconsistent data formats.

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