![]() |
Page History
...
Section | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
| ||||||||||
Current NCI Standard CRFsThe NCI develops and publishes standard CRF templates for use in creating new clinical trials protocol forms. Each CRFs consists of CDEs organized into 3 sections: mandatory, optional, and conditional CDEs. To retrieve these and any other forms registered in caDSR since the dates listed below, please visit the caDSR Form Builder, where a Guest account and password are provided for your convenience.
|
...
Section | ||
---|---|---|
| ||
CDEs InitiativesCDEs are organized in the caDSR CDE Browser based on Context and Classification Scheme. Opening up the Context name in the browser will reveal a "Classifications" node, that when opened will list all the projects in alphabetical order. Clicking on a project node will search for all CDEs used by the project. |
TCGA Phase II meta data elements (CDEs)
TCGA (The Cancer Genome Atlas) is a project funded by the National Cancer Institute (NCI) and National Human Genome Research Institute (NHGRI). A project overview can be found on the TCGA Home Page.
TCGA provides data element descriptions for the clinical data elements found in the TCGA data files. The BCR on-line data dictionary displaying the essentials of the clinical CDEs as an HTML page is located here. The files below contain all the caDSR metadata for these CDEs. The HTML data dictionary was generated from the XML download of the TCGA CDEs. For more information or help creating your own HTML Data Dictionary from NCI registered CDEs, please contact the NCI Help Desk.
They are also available from the CDE Browser in the caBIG Context under the Classifications tab heading "TCGA 2.6 by Disease". New TCGA CDEs not yet in the BCR data dictionary can be found under the caBIG Classification "The Cancer Genome Atlas", sub-heading "New TCGA Data Elements"
- TCGA Phase II CDEs in Excel - as of Oct. 19, 2011
- TCGA Phase II CDEs in XML - as of Oct. 19, 2011
North American Central Cancer Registries (NAACCR) meta data elements (CDEs)
NAACCR develops and promotes uniform data standards for cancer registration, and aggregates and publishes data from central cancer registries. It promotes the use of cancer surveillance data and systems for cancer control and epidemiological research. See their website for more information about NAACCR.
NCI has registered several versions of the NAACCR data elements as CDE metadata in caDSR for discovery and use by those wishing to utilize the NAACCR data, or create data repositories of compatible data.
The following versions of NAACCR have been recorded in caDSR, are available from the CDE Browser in the PS&CC Context under the Classifications tab heading "Division of Cancer Control and Population Sciences". They have been downloaded and made available here for convenience.
- NAACCR 11.1 CDEs in Excel - as of Dec 17, 2010
- NAACCR 11.1 CDEs in XML - as of Dec 17, 2010
- NAACCR 12.1 CDEs in Excel - as of April 23, 2012
- NAACCR 12.1 CDEs in XML - as of April 23, 2012
Surveillance, Epidemiology and End Results (SEER) meta data elements (CDEs)
...
For prior downloaded versions of the files see the Attachments listed at the end of this page. If importing caDSR content into another ISO/IEC 11179 registry, i.e. local implementation of cgMDR, please add the caDSR Registration Authority Identifier (RAI) 2.16.840.1.113883.3.26.2 to the metadata to keep the caDSR content distinct from the local repository. Per ISO/IEC 11179, the RAI is part of a globally unique identifier known as the IRID (Item Registry Identifier), and uniquely identifies registry content as being related to particular registrars. The IRID for all caDSR content is the <caDSR OID + Item public Id + item version>. For example, if the caDSR item public id = 2181292, version = 1.1, when importing you would add the RAI, and the result would be an IRID = 2.16.840.1.113883.3.26.2 + 2181292 + 1.1.
|
...
|
...
|
...
|
...
|
...
Biomedical Research Integrated Domain Group (BRIDG) meta data elements (CDEs)
BRIDG is a model that was created by a collaborative effort engaging stakeholders from the Clinical Data Interchange Standards Consortium (CDISC), the HL7 BRIDG Work Group, the US National Cancer Institute (NCI), and the US Food and Drug Administration (FDA). A logical information model was developed to describe basic, pre-clinical, clinical, and translational research. Please visit the BRIDG website for more information.
The CDEs in the BRIDG model are available from the CDE Browser in the BRIDG Context under the Classifications heading "Link to BRIDG 3.2", subheading "BRIDG 3.2". They have been downloaded and made available here for convenience.
- BRIDG 3.2 in Excel - as of Aug. 11, 2015
- BRIDG 3.2 in XML - as of Aug. 11, 2015
BRIDG 3.0.2 is also available in the Attachments section of this page and in the CDE Browser.
National Biomedical Imaging Archive (NBIA)(formerly NCIA)
...
|
...
|
...
|
...
|
...
|
...
|
...
|
...
- eMerge CDEs in Excel - as of August 05, 2015
- eMerge CDEs in XML - as of August 05, 2015
For prior downloaded versions of the files see the Attachments listed at the end of this page.
If importing caDSR content into another ISO/IEC 11179 registry, i.e. local implementation of cgMDR, please add the caDSR Registration Authority Identifier (RAI) 2.16.840.1.113883.3.26.2 to the metadata to keep the caDSR content distinct from the local repository. Per ISO/IEC 11179, the RAI is part of a globally unique identifier known as the IRID (Item Registry Identifier), and uniquely identifies registry content as being related to particular registrars. The IRID for all caDSR content is the <caDSR OID + Item public Id + item version>. For example, if the caDSR item public id = 2181292, version = 1.1, when importing you would add the RAI, and the result would be an IRID = 2.16.840.1.113883.3.26.2 + 2181292 + 1.1.
...
|
Section |
---|
REDx - caDSR REDCap Transformation Utilities
|
Attachments |
---|
Wiki Markup |
---|
{scrollbar:icons=false} |