CDE Catalog | NINDS Common Data Elements

***Please contact the NINDS CDE Team (NINDSCDE@emmes.com) if you encounter any search difficulties.***

The CDE Catalog is a directory of the available NINDS CDEs. Users can search the Catalog to isolate a subset of the CDEs (e.g., all stroke-specific CDEs, etc.), and to view and download details about the CDEs.

Select any filter below to search the CDE Catalog.

For best results, clear form between searches. In addition, when specifying NeuroRehab, Sport-Related Concussion (SRC) or Traumatic Brain Injury (TBI) as the Disease, please select a Subdisease as well.

NeuroRehab Comprehensive includes all NeuroRehab CDE recommendations. NeuroRehab General includes all NeuroRehab CDE recommendations that are not disease specific. All other NeuroRehab Subdiseases include recommendations specific to existing NINDS CDE project disorders.

Choose your Time Frame for your SRC study (Acute (time of injury until 72 hours), Subacute (after 72 hours to 3 months), and Persistent/Chronic (3 months and greater post-concussion) or Comprehensive if your study falls across the study time frames.

Choose your type of TBI study (Acute Hospitalized, Concussion/Mild TBI, Moderate/Severe TBI: Rehabilitation, or Epidemiology) or Comprehensive if your study falls outside of the study types or incorporates aspects of more than one type of study.

Search Form

CRF Name

Displaying 76 - 100 of 883

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Operations

Selected 25 rows in this page.

The search results below can be downloaded by clicking the checkboxes on the far left side of the table. Select the header checkbox to select all CDEs listed on the first page. Then choose CDE Detailed Report from the Choose an operation dropdown menu.
Select all	CDE ID	CDE Name	Definition	Classification	CRF Name	Copyrighted or trademarked	Disease Name	Subdisease Name
F1120-C14513	C14513	Device implanted negative electrode location text	The location of negative electrodes from the implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1122-C18571	C18571	Device implanted nerve stimulator new component model number	The model number of the new implanted nerve stimulator (INS) component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18572	C18572	Device implanted nerve stimulator new component registration number	The registration number of the new implanted nerve stimulator (INS) component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18565	C18565	Device implanted nerve stimulator revision component type	The modification of implanted nerve stimulator (INS) components including explant, replacement, and repositioning	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18569	C18569	Device implanted new extension component model number	The model number of the new extension component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18570	C18570	Device implanted new extension component registration number	The registration number of the new extension component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18573	C18573	Device implanted new lead component model number	The model number of the new lead component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18574	C18574	Device implanted new lead component registration number	The registration number of the new lead component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18558	C18558	Device implanted other adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to other Adverse Event (AE), specification	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1122-C18558	C18558	Device implanted other adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to other Adverse Event (AE), specification	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1121-C18558	C18558	Device implanted other adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to other Adverse Event (AE), specification	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1122-C18576	C18576	Device implanted other new component model number	The model number of the other, unspecified new component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18577	C18577	Device implanted other new component registration number	The registration number of the other, unspecified new component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18578	C18578	Device implanted other revision component type	The modification of the other, unspecified component including explant, replacement, and repositioning	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18955	C18955	Device implanted other text	The free-text field related to 'Device implanted type' specifying other text. The type of device used	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18955	C18955	Device implanted other text	The free-text field related to 'Device implanted type' specifying other text. The type of device used	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1121-C18955	C18955	Device implanted other text	The free-text field related to 'Device implanted type' specifying other text. The type of device used	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1120-C14510	C14510	Device implanted positive electrode count	The number of positive electrodes used by the implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C14511	C14511	Device implanted positive electrode location text	The location of positive electrodes from the implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C14507	C14507	Device implanted pulse width value	The width of the electrical pulse as set in the implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C14503	C14503	Device implanted removal date	The date the device no longer provided therapy according to the parameters specified	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1122-C14532	C14532	Device implanted revision component model number	The model number, lot number, or serial number of the replacement/new component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C14533	C14533	Device implanted revision component registration number	The registration number or serial number of the new component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C14530	C14530	Device implanted revision component type	The name of the components of the device that were modified or replaced	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C14529	C14529	Device implanted revision modification date	Date (and time, if applicable and known) of the device revision if replacement or modification occurred	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy

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The NINDS CDE Team does not post proprietary instruments/scales recommended by the CDE Working Groups on this website. This includes, but is not limited to, copyrighted or trademarked instruments/scales. Information about recommended instruments can be found in the Notice of Copyright (NOC) documents under ‘CRF Module/Guideline’ on each disorder’s data standards page. For any questions regarding these instruments/scales please contact the corresponding owner/author. The NINDS CDE Team is not responsible for the availability or content of these external sites, nor does the NINDS CDE Team endorse, warrant or guarantee the products, services or information described or offered at these other internet sites.