Record the patient's lab results.
Patients on NCI/CCR's intramural studies who have their labs drawn at the Clinical Center will use the Lab Load Interface (LLI) tool to select which labs results to electronically transfer into C3D. The selected results are then loaded onto the appropriate Lab Panel CRFs overnight. Instructions on how to use the LLI tool are in appendix IV.
2007 and earlier C3D Studies, in general, do not use the LLI tool and labs done in the Clinical Center are automatically loaded directly in C3D.
It takes at least 48 to 72 hours for Clinical Center Labs to become available to C3D.
Outside labs need to be manually entered in C3D. Refer to the 'Inserting Unplanned Visits' section of the General Instructions of this manual.
It is common to have several forms of the same kind of lab for a patient. Click on the C3D RDC worksheet column header labeled "Show unplanned visit" to see all these extra lab results.
The following table lists the standard lab CRFs and appendix III the tests in each of them. The C3D Study will have only the appropriate lab CRFs as specified by the Protocol.
• Blood Chemistries
• Respiratory Functions
• Blood Gases
• Bone Marrow
• Lymphocyte Phenotype
• Serum Electro
• Chimerism Lab
• Other Serum Chemistries
• Other Urinary Results
• Urine Immune Electro
Description / Instructions
Enter the date the lab sample was collected.
Enter the lab sample collection time in military format (24 hours). Seconds are optional and default to 00 if not entered.
Ex: 13:56:00 (for 1:56:00 PM)
Select the source of the lab results.
Use pick list.
Indicates the course number this lab is related to.
Day in Course(d)
Indicates the day since the beginning of course this lab is related to.
Pre-defined name of the lab test. Each lab panel has a different set of tests which are listed at the appendix III.
Enter the lab test result value as reported.
Select the appropriate lab test value unit of measurement.
Use pick list.
For labs loaded from the MIS/CRIS system, the range is automatically populated.
Indicates how the lab result value compares to the lab test normal range.
Derived from the lab test result value and the lab test ranges from the version of the NCI Common Terminology Criteria for Adverse Events (CTCAE) specified by the Protocol.
Derived from lab test result value.
Value in Preferred UOM(d)
Derived the lab test result value in the preferred unit of measurement which is pre-defined by the institute.
The preferred unit of measurement for the specified lab test.
Legend: (d) derived field, (m) RDC mandatory, (c) for CTEP reporting only.
Lab test has grade higher than zero or than the most recent baseline lab test grade but no relevant Adverse Event exists.
Correct the lab grade or make sure a relevant Adverse Event exists.
Two labs exist for the same date and time.
Review both labs and delete/correct one of them.
Course number is derived from the course initiation start date and the lab date (visit date).
Day in Course
Number of days since the beginning of the course is derived from the course initiation start date and the lab date (visit date).
Derived based on the lab value result and normal high/low range.
Derived from the lab test result value, unit of measurement and the lab test normal range.