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Submitting Accruals at the Subject Level for Non-Interventional Trials
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Study Subject Information
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Instruction/Description
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Study Subject ID*
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Enter the unique Patient ID as per the lead organization or the study site where the subject is registered.
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Study Subject Birth Date*
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Enter the subject's month and year of birth in the format MM/YYYY .
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Study Subject Gender*
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Select the subject’s gender. If gender information is not available, select Unknown.
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Study Subject Race*
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Select one or more values for race.
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To select multiple races, select one race, and then press and hold the CTRL/CMD key as you select the other(s). |
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Study Subject Ethnicity*
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Select a value for ethnicity.
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Study Subject Country*
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Select the subject’s country of origin.
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Study Subject Zip Code
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Enter the subject’s Zip Code if known. This field is mandatory if the country of origin is United States.
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Registration Date*
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Enter the date that the subject was registered for the trial.
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Study Subject Method of Payment
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For United States study subjects only, select the appropriate payment method.
Site*
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Click Look Up, and follow the instructions in Selecting Sites for Study Subject Records Using ICD-O-3 Codes.
Mandatory for ICD-O-3 trials unless you record a CD-O-3 Disease Code. Optionally, record both Site and Disease codes. Site codes are available at http://training.seer.cancer.gov/head-neck/abstract-code-stage/codes.html.
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Disease*
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Click Look Up, and follow the instructions in Selecting Diseases for Study Subject Records.
Mandatory for ICD-9 and SDC trials; and for ICD-O-3 trials unless you record a CD-O-3 Site Code.
Use Histology codes when C codes are not available (for example, for Multiple Myeloma, NHL, Leukemia).
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Participating Site*
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Select the appropriate site from the drop-down list.
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You can submit accrual data to the NCI CTEP's Clinical Data Update System (CDUS) on a quarterly basis (i.e., December 31, March 31, June 30) up to 30 days following the end of the quarter. For Complete trials, lead organizations report all subjects accrued for the trial (both in the lead organization and in all participating sites). For Abbreviated trials, each participating site reports the number of its own accruals (accrual count) only. |
Submitting Accruals at the Summary Level for Non-Interventional Trials
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Each participating site can submit/update the number of patients accrued to date per trial.
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Select the trial you want to work with by following instructions in Searching for and Selecting Your Trials, and clicking the corresponding NCI Trial Identifier link. The Participating Site Subject Accrual Count page appears. If no accrual counts have been recorded for this trial previously, you can elect to submit your accrual data at the subject level instead of the summary level.
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