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caDSR Wiki | caDSR Database and Tools | caDSR Documentation
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NCI Standard CDEs
- All production CDEs with Registration Status = "STANDARD" as of Sept 24, 2014
caDSR Community Released CDEs
- All non-retired production CDEs (CDEs with Workflow status NOT = "RETIRED....") as of July 29th, 2015
REDx - caDSR REDCap Transformation Utilities
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- User Guide
REDxCDE V3
- Transformation utility to convert caDSR CDE Browser 4.0.5 XML download format into REDCap Data Dictionary as of 2014/11/10
- Version 3 - 2015-08-05: Change field note to contain the CDE Question Text, the field does not need to be lower-case without spaces, that rule applies only to variable name
- Version 2.1 - 2015-6-18: Add instruction for customizing Form name, Id and Version
- Version 2.0 - 2015-6-10: Add a check for existing CDE PV Values. If already a numeric, use existing value. If not, generate a unique value based on the position in the value list.
REDxCRF Single V5.0
- Transformation utility to convert a single caDSR Form Builder 4.0.3.1 formCart Version 1 XML format (retrieved from Objcart API) into REDCap Data Dictionary
- Version 5 - 2015-07-29: Add a check for existing CDE PV Values. If PV Value is already a numeric, use existing value. If not, generate unique value based on the position of the PV in the value list.
- Version 4 - 2014-11-10:
- Change generation of Field Label to the original caDSR Preferred Question Text, without converting it to lower case and replacing spaces with underscores
- See Version comments within the xslt for prior version release notes
Current Standard CRF Downloads:
Adverse Event and Series Adverse Event NCI CRF Standards created on September 5th, 2014
Concomitant Medication NCI CRF Standards created on September 5th, 2014
Consent NCI CRF Standards created on October 4th, 2013
CT Image Acquisition NCI CRF Standards created on December 9th, 2013
CT Imaging Agent NCI CRF Standards created on December 9th, 2013
Demography NCI CRF Standards created on March 22nd, 2013
Diagnosis NCI CRF Standards created on December 9th, 2013
Diagnosis Administrative NCI CRF Standards created on October 4th, 2013
Diagnosis Gross Pathology NCI CRF Standards created on December 9th, 2013
Diagnosis Intervention NCI CRF Standards created on January 7, 2014
- Diagnosis Metastasis NCI CRF Standards created on December 9th, 2013
- Diagnosis Microscopic Pathology NCI CRF Standards created on December 9th, 2013
- Eligibility NCI CRF Standards created on October 4th, 2013
- End of Form NCI CRF Standards created on June 29th, 2012
- Enrollment NCI CRF Standards created on August 3rd, 2012
- Equipment NCI CRF Standards created on October 18th, 2013
- Follow-up NCI CRF Standards created on December 9th, 2013
- Footer NCI CRF Standards created on August 3rd, 2012
- Header NCI CRF Standards created on June 29th, 2012
- Image Administration NCI CRF Standards created on December 9th, 2013
- Image Quality NCI CRF Standards created on October 4th, 2013
- Laboratory Test Results NCI CRF Standards created on September 5th, 2014
- Lost to Follow-Up NCI CRF Standards created on December 9th, 2013
- Medical History NCI CRF Standards created on June 29th, 2012
- Off Study NCI CRF Standards created on October 4th, 2013
- Off Treatment NCI CRF Standards created on October 4th, 2013
- Outcome Measures NCI CRF Standards created on January 28th, 2013
- Participant Identification NCI CRF Standards created on February 5th, 2014
- PET Emissions Scan NCI CRF Standards created on November 1st, 2013
- PET Equipment QC Assessment NCI CRF Standards created on October 4th, 2013
- PET Imaging Agent NCI CRF Standards created on April 7th, 2014
- PET Patient Prep NCI CRF Standards created on October 4th, 2013
- Physical Examination NCI CRF Standards created on August 3rd, 2012
- Prior Post (Other) Therapies NCI CRF Standard created on Septemer 5th, 2014
- Progression NCI CRF Standards created on December 9th, 2013
- Protocol Deviations NCI CRF Standards created on August 15th, 2012
- Radiation NCI CRF Standards created on May 8th, 2014
- RECIST NCI CRF Standards created on May 11th, 2015
- Registration NCI CRF Standards created on June 29th, 2012
- Response NCI CRF Standards created on December 9th, 2013
- Screening NCI CRF Standards created on October 4th, 2013
- Staging/Extent of Disease NCI CRF Standards created on September 5th, 2014
- Staging/Extent of Disease NCI CRF Standards created on January 7th, 2014
- Staging/Extent of Disease NCI CRF Standards created on October 9th, 2013
- Staging/Extent of Disease NCI CRF Standards created on March 22nd, 2013
- Staging/Extent of Disease NCI CRF Standards created on June 29th, 2012
- Staging/Extent of Disease NCI CRF Standards created on June 29th, 2012
- Staging Cervix Uteri NCI CRF Standards 3443295 in Excel
- Staging Colon and Rectum NCI CRF Standards 3443381 in Excel
- Staging Corpus Uteri Sarcoma NCI CRF Standards 3446968 in Excel
- Staging Fallopian Tube NCI CRF Standards 3447481 in Excel
- Staging Leukemia NCI CRF Standards 3461076 in Excel
- Staging Lymphoma (Including Hodgkins) NCI CRF Standards 3461103 in Excel
- Staging Ovary NCI CRF Standards 3443610 in Excel
- Staging Soft Tissue Sarcoma NCI CRF Standards 3443747 in Excel
- Staging Stomach NCI CRF Standards 3444235 in Excel
- Staging Thyroid NCI CRF Standards 3461837 in Excel
- Staging Vagina NCI CRF Standards 3451637 in Excel
- Staging Vulva NCI CRF Standards 3448033 in Excel
- Staging/Extent of Disease NCI CRF Standards created on August 15th, 2012
- Study Agent Administration NCI CRF Standards created on September 5th, 2014
- Surgery NCI CRF Standards created on September 5th, 2014
- Survival NCI CRF Standards created on December 9th, 2013
- Vital Signs NCI CRF Standards created on October 4th, 2013
Standard CDEs by Project
TCGA Phase II Data Elements - as of Oct. 19, 2011
North American Central Cancer Registries (NAACCR) meta data elements (CDEs)
- 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) - as of Dec 23, 2010
BRIDG metadata elements (CDEs) - as of Feb 03, 2011
National Biomedical Imaging Archive (NBIA)(formerly NCIA)- as of Feb 09, 2011
Health Information National Trends Survey (HINTS2005)- as of April 04, 2012
eMerge Project - as of August 05, 2015 (see page Attachments for collection as of April 04, 2012)
For other formats and prior 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.
Coming soon! A link to cancerGrid UK cgMDR PTCRi (Particle Therapy Cancer Research) instance of cgMDR where you can download metadata elements in caDSR XML format, the native cgMDR format for importing into your own cgMDR instance, as well as an XML Schema annotated with W3C SAWSDL annotation tags.
The following lists the attachments to this page.
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Attempting to download all the caDSR CDEs would result in a file size that is too large for a single MS Excel download, and currently forms can only be downloaded one form at a time.
Therefore, "canned", or pre-downloaded collections of all the NCI "Released" CDEs, and CDEs by selected individual projects in is provided for your convenience. The NCI Preferred Standards have become too large to download in a single file, so they can be extracted from the "Released" CDE files.
Note that NCI added an FTP site where all "Released" CDEs as XML.
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REDCap CDE and CRF Transformation Utilities - REDx
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Current NCI Standard CRFs
The 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.
There are currently over 70 Standard CRFs released for production use.
There are 60 CRFs that have been converted to REDCap format and can be found in the Shared Library, and in the zip file attached here.
NCI Standard CRFs: REDCap format Zip
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CDEs Initiatives
CDEs initiatives are owned by individual NCI Divisions, Offices, and Centers, as well as by NCI stakeholder communities who have chosen to use NCI caDSR as a central repository for their CDEs. The CDEs are organized in the caDSR CDE Browser based on Context and Classification Scheme. Contexts represent a community who have agreed to share CDEs and CRFs, within a Context end users create Classification Schemes within caDSR for various projects in their community, and use them to classify and organize CDEs. The classifications are a list of keywords and categories familiar to the community. Opening up a Context in the CDE Browser will reveal a "Classifications" node, that when opened will list all the projects in alphabetical order. Clicking on a project node will return a list of all the CDEs for that project.
For prior downloaded versions of these collections, see the Attachments listed at the end of this page. The date of the download is listed as the "as-of" date for each collection of CDEs.
If importing caDSR content from a download into another ISO/IEC 11179 or other similar CDE or CRF metadata registry, 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.
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caDSR Wiki | caDSR Database and Tools | caDSR Documentation
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