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  1. Select the study you want to work with by following instructions in Searching for and Selecting Your Trials, and clicking the corresponding NCI Trial Identifier link. The Search Study Subject page appears.
     
  2. Click Add Study Subject.
    The Add Study Subject panel appears right-aligned to the Study Subject page. (Screenshot below displays Subject accrual)

  3. Enter the required demographic information in the text fields and drop-down lists. An asterisk (*) indicates a required field. 

  4. The following table describes the valid values and formats for each field.

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    Accrual Data Elements for Complete Trials
    Accrual Data Elements for Complete Trials

    Include Page
    Accrual Data Elements Table with CTRP-Accepted Values for Complete Trials - Include v4.8
    Accrual Data Elements Table with CTRP-Accepted Values for Complete Trials - Include v4.8

  5. Click Save.
    The study subject record appears in the List of Study Subjects.
Tip

For CompleteComplete studies, lead organizations report all subjects accrued for the study (both in the lead organization and in all participating sites). For Abbreviated studies, each participating site reports the number of its own accruals (accrual count) only. 

  • If your organization currently reports subject accrual information for studies to CTEP or DCP via the CDUS/OPEN systems, continue to report subject accrual information via CDUS/OPEN. The NCI will manage the transfer of subject accrual data for CDUS/OPEN studies internally. Otherwise, report your organization's subject accrual data to CTRP.