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Accessing routinely collected health data to improve clinical trials: recent experience of access.

Archie MacnairSharon B LoveMacey L MurrayDuncan C GilbertMahesh K B ParmarTom DenwoodJames R CarpenterMatthew Robert SydesRuth E LangleyFay H Cafferty
Published in: Trials (2021)
Our experience demonstrates that data access can be a prolonged and complex process. This is compounded if multiple data sources are required for the same project. This needs to be factored in when planning to use EHR within RCTs and is best considered prior to conception of the trial. Data holders and researchers are endeavouring to simplify and streamline the application process so that the potential of EHR can be realised for clinical trials.
Keyphrases
  • electronic health record
  • clinical trial
  • big data
  • healthcare
  • phase ii
  • phase iii
  • randomized controlled trial
  • quality improvement
  • risk assessment
  • data analysis
  • climate change