The following table describes the data elements displayed in the CTEP PCD report for each trial:
Data Element | Description |
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NCI ID | unique ID assigned to the trial by the CTRP. |
CTEP ID | The unique ID assigned to the trial submitted by CTEP (Cancer Therapy Evaluation Program). |
PCD | date that the final subject was (or will be) examined or received (or will receive) an intervention for the purposes of final collection of data for the primary outcome, whether the clinical trial concluded according to the prespecified protocol or was terminated (as specified in US Public Law 110-85, Title VIII, Section 801, with respect to an applicable clinical trial). |
PCD Type | value indicating whether the completion date is the one on which the trial is expected to complete (Anticipated), or the date on which it actually completed (Actual). |
Sponsor | name of the primary organization that oversees the implementation of the study and is responsible for data analysis, as defined in 21 CFR 50.3. |
Sponsor PO ID | Identifier assigned to the sponsor by the CTRP. |
Lead Organization | name of the organization responsible for the trial's research protocol, and responsible for the overall scientific and administrative coordination, study monitoring, and data management activities of the trial. |
Lead Org PO ID | Identifier assigned to the lead organization by the CTRP. |
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Study PI PO ID | Identifier assigned to the PI by the CTRP. |
CTRP Site Admin | The name of each site administrator on the trial, as specified in CTRP. This column also includes the phone number and email address of each site administrator. |
Type | Value indicating why the report includes the trial:
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