Hours and seating at library facilities are limited at this time. Learn more about our safe and smart RESTART here.
Group study spaces have been repurposed to facilitate proper physical distancing. Learn more about our safe and smart RESTART here.
Librarians are available to offer virtual assistance 7 days a week.
Additional help options can be found on our Ask Us page.
registry and curated database containing the basic set of data items deemed essential to describe a study at inception, as per the requirements set out by the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) and the International Committee of Medical Journal Editors (ICMJE) guidelines. All study records in the database are freely accessible and searchable and have been assigned an ISRCTN ID. The Terms and Conditions enable anyone to cite with attribution the details in each study record, and encourage unrestricted use of all metadata generated during the process of registration, updating or reporting. Requires registration.
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