Research Registration Dataset
This is the research information that must appear in a register in order for a given research to be considered fully registered. WHO has recommended a minimum of 20 items in the WHO Trial Registration Data Set—mainly intended for clinical trials. However, countries may choose to have additional items for their National Registries, tailored to their specific needs. WHO primary registry in the International Clinical Trials Registry Platform (ICTRP) must have at least the minimum 20 data items recommended in the Trial Registration Data Set.