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How to Register New Complete Trials

  1. Perform a search for the trial. For instructions, refer to Searching for Trial Records. If

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MultiExcerptNamesubmittrial

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  1. the trial does not already exist

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  1. , proceed to the next step. (The system uses the Lead Organization ID, Lead Organization Trial ID, and the ClinicalTrials.gov Identifier to detect duplicates. If the system detects a duplicate

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  1. , the system

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  1. does not record your trial.)

How to Register New Complete Trials

  1. On the toolbar, click Register Trial, and select your trial's Submission Category (funding source) from the drop-down list, either National, Externally Peer-Reviewed, or Institutional. (For information, refer to CTRP Trial Categories, Study Sources.)

    Tip

    To read a definition of each of the trial submission categories (study sources), click View Trial Category Definitions, click the Help icon (Help icon, circle shape with a question markImage Modified) next to each category, or refer to

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  1. https://cancercenters.cancer.gov/GrantsFunding/

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  1. eData#dt4.


    Register Trial menu with trial submission categoriesImage Modified

    The Register Trial page appears. 

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    Tip
    titleYou can expand and collapse sections of the registration page

    By default, all sections of the registration form are displayed. 

    To collapse or  expand each section individually, click the Collapse or Expand icon on the right side of the section title as shown in the figures below.

    To collapse all sections, click Collapse All.

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  2. In the various fields, specify

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  1. the appropriate information

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  1. . The following table describes the fields.

    Tip
    titleTip

    Be sure to provide information for all fields marked with an asterisk (*). If you cannot complete the registration of a trial in one Registration session, you can save a draft of the trial details you have completed. (Refer to "Save as Draft" below.) Later you can return to complete the registration in another session.


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Instructions for registering Complete trials

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XML required. Enable "Upload from NCI CTRP" in ClinicalTrials.gov?

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If you require an XML document to register your trial with ClinicalTrials.gov, select Yes.
If you are not going to submit your trial to ClinicalTrials.gov, select No.
The option you select here dictates which sections you will be required to complete. For example, if you select No, you will not be required to complete responsible party and regulatory information. If you select Yes, NCI will be added as a collaborator to the Funding Source.

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  1. Field LabelDescription/Instructions

    Various

    In the various fields, specify information as

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    Save as Draft

    Click to save a draft of the record so that you can complete the registration at another time. You must have provided, at the minimum, both the Lead Organization and Lead Organization Trial Identifier to save a draft.
    The system saves your draft, assigns it a unique ID (for tracking purposes), and sends you an email message confirming that the information has been saved. You can end your Registration session and retrieve your draft later to complete the registration.

    Review Trial

    Cancel

    Click to cancel the registration. A pop-up message prompts you to confirm cancellation.

    Note

    If you choose to cancel the registration, you will lose all data that you may have entered

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  1. .

  2. To continue with the trial registration, scroll to the bottom of the Review Trial Details page, and then click Submit. To prevent creating a duplicate record, do not click Submit more than once. If you have to make changes after you click Submit, contact the CTRO at ncictro@mail.nih.gov rather than using your browser's Back button to make changes.
    The registration notification message system sends you an email message to acknowledge that the trial has been submitted. Later it sends another email message to notify you when your trial has been accepted or rejected.

Info

After submission, most users other than the trial submitter can not see the trial information you provided until the information has been validated. However, an organization administrator (if one exists) and an assigned owner can access the information prior to validation.