{"id":2741,"date":"2022-03-08T09:20:13","date_gmt":"2022-03-08T08:20:13","guid":{"rendered":"https:\/\/www.we4cr.com\/clinicaltrials-gov\/"},"modified":"2025-09-01T15:52:34","modified_gmt":"2025-09-01T13:52:34","slug":"clinicaltrials-gov","status":"publish","type":"glossary","link":"https:\/\/www.we4cr.com\/it\/glossary\/clinicaltrials-gov\/","title":{"rendered":"Clinicaltrials.gov"},"content":{"rendered":"<p>Every trial must be recorded in a publically accessible database before the study starts, or within 30 days from its start. Clinicaltrial.gov is the most common site. A registered user can submit the study on the database, following the instruction provided in the webpage. At the end of the process, the study will be assigned a unique code that can be used in all official documentation as a reference number for the study (when applicable). 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