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 801 - 825 of 883

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
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
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-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-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-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-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-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
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
F1120-C14512	C14512	Device implanted negative electrode count	The number of negative electrodes used by the implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C14514	C14514	Device implanted modification reason	The reason for modification of parameters or electrode configuration of original implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C18954	C18954	Device implanted modification other text	The free-text field related to 'Device implanted modification reason' specifying other text. The reason for modification of parameters or electrode configuration of original implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C18557	C18557	Device implanted log line number	The reference line number of the entry on the implanted device log	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1122-C18568	C18568	Device implanted left lead revision component type	The modification of the left lead component including explant, replacement, and repositioning	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1122-C18567	C18567	Device implanted left extension revision component type	The modification of the left extension component including explant, replacement, and repositioning	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18556	C18556	Device implanted intolerable stimulation adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to intolerable stimulation related Adverse Event (AE), specification	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1121-C18556	C18556	Device implanted intolerable stimulation adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to intolerable stimulation related Adverse Event (AE), specification	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1122-C18556	C18556	Device implanted intolerable stimulation adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to intolerable stimulation related Adverse Event (AE), specification	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1121-C14516	C14516	Device implanted implant date and time	Date (and time, if applicable and known) the device was implanted and became functional	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1120-C14506	C14506	Device implanted frequency	The electrical frequency (number of complete cycles of a periodic process occurring per unit time) as set in the implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C18555	C18555	Device implanted comment text	The free-text field to capture any comments related to an implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C14504	C14504	Device implanted amperage value	The electrical amperage (amplitude) as set in the implanted device (strength of the electric current)	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1121-C14527	C14527	Device discontinuation reason	The reason the subject discontinued use of the device	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C18959	C18959	Device discontinuation other text	The free-text field related to 'Device discontinuation reason' specifying other text. The reason the subject discontinued use of the device	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14518	C14518	Device component type	The name of a part of the device that has a registration number or serial number	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14519	C14519	Device component registration or serial number	The registration number or serial number of the device and component(s) to distinguish it from other devices (extension if applicable)	Supplemental	Devices Log	False	Epilepsy	Epilepsy

Displaying 801 - 825 of 883

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.