NLM Technical Bulletin, May-Jun 2024, Study Record Information Displays in the Modernized ClinicalTrials.gov

ClinicalTrials.gov study records consist of required and optional data elements that summarize a study's protocol and results information. Sponsors and investigators submit the information for their studies during registration and results reporting, respectively. Over the past 25 years, the data elements and their requirements have changed in response to the evolution of trial reporting laws and policies. Consequently, older ClinicalTrials.gov records may be missing information that was not being collected or was optional during initial submission but was subsequently added or became required. As we modernized the ClinicalTrials.gov website, we considered the display of information and the related explanations that would be most helpful to users, including how to display the data submitted by study sponsors and investigators and how to indicate the information they did not provide.

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NLM Technical Bulletin, May-Jun 2024, Study Record Information Displays in the Modernized ClinicalTrials.gov

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