Cancer Center

CTRP Organization Family Name.

The CTRP Data Table 4 report uses the CTRP Family-Organization relationships to select trials for a report.  Reports are based on a Cancer Center Family.  All trials for which the Family organizations or affiliates are participating sites are included in the report.

P30 Grant Number

Clinical Research Cat

Clinical Research Category as follows:

• INT = Interventional trial
• OBS = Observational, non-interventional trial
• ANC/COR = Ancillary/Correlative non-interventional trial

Study Source

CTRP Data Table 4 Funding Category as follows:

• N = National
• E = Externally Peer-Reviewed
• I = Institutional
• D, N, E, I for Industrial trials based on the following:
  
  • D = Industrial trials other than Consortia trials
  • N = Industrial Consortia trials, National
  • E = Industrial Consortia trials, Externally Peer-Reviewed’
  • I = Industrial Consortia trials, Institutional

Specific Funding Source

CTRP organizations listed as Data Table 4 Funding Sponsor for the trial.

Primary Site

Data Table 4 Anatomic Sites for the trial.

Protocol ID

Lead Org ID.

Multiple IDs, including the following:

• NCI
• CTEP or DCP
• Other IDs

Is Multi Institutional?

Indicates whether there is more than one Cancer Center participating in the trial, as follows:

• Y (Yes) = There is more than one Cancer Center participating in the trial.
• N (No) = There is only one Cancer Center participating in the trial.

PI (Principal Investigator) - Last Name, First Name, MI

Last name, first name, and middle initial of the Principal Investigator (PI) for the trial or participating site, as follows:

• If a member of the specified Cancer Center Family is the lead organization of the trial, the report displays the name of the PI for the trial.
• Otherwise, the report displays the name of the PI for a participating site, as follows:
  
  • If only one member of the specified Cancer Center Family is a participating site on the trial, the report displays the name of the PI for that site.
  • Otherwise, the report displays the name of the PI for the first participating site with the Organizational affiliation (the first one added to the trial).

Prog(ram) Code

A code assigned by the Cancer Center to each participating site on a trial to classify the type of cancer research being conducted by the trial at that site.

Open Date

Date on which the trial status became Active within the date range given.

Close Date

Date on which the trial status was Closed to Accrual or Closed to Accrual and Intervention.

Phase

Primary Purpose

Primary purpose the trial, as follows:

• Tre = Treatment
• Pre = Prevention
• Sup = Supportive Care
• Scr = Screening
• Dia = Diagnostic
• Hsr = Health Services Research
• Bas = Basic Science
• Dev = Device Feasibility
• Oth = Other

For more information about these values, refer to Recording Trial Details.

Official Title

Official name of the protocol provided by the study principal investigator or sponsor

The participating site (Cancer Center) target accrual. The system displays this value if available in CTRP for the trial. For instructions on specifying this information in CTRP, refer to Managing Targeted Accrual. However, if the value is not available in CTRP, it should be reported under this column if otherwise available.

Total number of subjects accrued for the trial for all organizations in the Cancer Center Family with the relationship “Organization” for the time period you selected.

If detailed accrual information was reported for the trial, the system calculates accrual within the specified time period (such as 12 months): 

• If a cut-off date is available, the system calculates accrual based on the cut-off date.
• If a cut-off date is not available, the system uses the Subject Registration Date as the cut-off date.

If summary accrual was reported (such as for Industrial trials), the system calculates accrual for a selected time period based on the difference between the last summary accrual reported before the time period and the last summary accrual reported within the time period. If no summary accrual was reported before the time period selected, the system displays the last summary accrual reported within the time period as the accrual count for the time period.

Total number of subjects accrued to date for the trial for all organizations in the Cancer Center Family with the relationship “Organization”.

Total number of subjects accrued for the trial for all organizations in the Cancer Center Family with the relationship “Affiliation” for the time period you selected.

If detailed accrual information was reported for the trial, the system calculates accrual within the specified time period (such as 12 months): 

• If a cut-off date is available, the system calculates accrual based on the cut-off date.
• If a cut-off date is not available, the system uses the Subject Registration Date as the cut-off date.

If summary accrual was reported (such as for Industrial trials), the system calculates accrual for a selected time period based on the difference between the last summary accrual reported before the time period and the last summary accrual reported within the time period. If no summary accrual was reported before the time period selected, the system displays the last summary accrual reported within the time period as accrual for the time period.

Total number of subjects accrued to date for the trial for all organizations in the Cancer Center Family with the relationship “Affiliation”.

In Jasper, this column is intentionally blank. To use this column:

1. Export the report to Microsoft Excel. For instructions, refer to Exporting Reports.
2. In the spreadsheet, add comments to this column.
3. Print the spreadsheet to PDF.