Research protocols submitted to the ED/SBS IRB need to be registered at Clinicaltrials.gov if publications resulting from this study will be published in a member journal of the International Committee of Medical Journal Editors (ICMJE) or in a publication that adheres to the standards of the ICMJE. (for example, studies investigating relationships between the health-related intervention and any health outcomes.) Please note that per the Revised Common Rule, one IRB-approved consent form used to enroll subjects must be posted by the awardee on a designated Federal public website for each clinical trial conducted or supported by a Federal department or agency.
If this does not apply, please check No to question 20.1.
Additional information can be found at https://kb.wisc.edu/gsadminkb/page.php?id=34044.