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Comment: Moved content to the new "Updating Trial Information" page.

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  • Editorial, Administrative Changes (correction of minor typographical errors; clarifications made to previously approved descriptions of research)
  • Data, Data Collection, and Data Collection Materials (revised study diaries; revised questionnaires or QOL surveys given to participants)
  • Recruitment of Subjects (changes in the way subjects are recruited; a new or revised advertisement)
  • Principal Investigator Contact Information

 

How to Update Trials

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Update Trial page for Industrial trials showing Participating Sites and Trial Related Documents sectionsImage Removed
Update Trial page for Industrial trials

Make changes to the fields as necessary. The system requires you to provide information for all fields marked with an asterisk (*). The instructions are the same for trial registration and trial update, with some exceptions:

If applicable, enter a ClinicalTrials.gov ID, and then click Add ClinicalTrials.gov Identifier

Note

You cannot change the ClinicalTrials.gov ID once you have added it. Also, if the trial record already has a ClinicalTrials.gov ID, you cannot change it. If the ClinicalTrials.gov ID specified for a trial is incorrect, contact the CTRO at NCICTRO@mail.nih.gov.

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Trial Details section of Update Trial page, annotated to show the alternate title indicatorImage Removed
To view the alternate titles, click the asterisk ( * )
Trial Alternate Titles listImage Removed

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A trial can accumulate program codes from different organization families. For example, a participating site might belong to a different organization family than the lead organization. When you update a trial, the Program Code field displays all codes from the master list for the organization family of the lead organization.

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Primary Completion Dates are optional for non-interventional trials and for DCP trials. In both cases, the system excludes such trials when submitting XML documents to ClinicalTrials.gov. Otherwise, Primary Completion Dates are required. 

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For instructions on recording each field otherwise, refer to Registering New Trials.

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