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 426 - 450 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-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-C14515	C14515	Device implanted type	The type of device used	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-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
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
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
F1120-C18559	C18559	Device implanted serious adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to serious device adverse effect(s) specification	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-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-C14515	C14515	Device implanted type	The type of device used	Supplemental	Devices 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
F1121-C14517	C14517	Device manufacturer name	The company responsible for development 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
F1121-C14520	C14520	Device stimulation target anatomic site	The target of stimulation the device acts upon (where the device lead is located)	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14521	C14521	Device lead type	Type of insulated wires (leads) for the device implanted	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14522	C14522	Device lead contact count	The number of contacts of the insulated wires (leads)	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14523	C14523	Device neurostimulator anatomic site	The location in the body of where the device is providing electrical stimulation	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14524	C14524	Device permanent explant date	Date the device was removed from the subject	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C14525	C14525	Device part left in the body indicator	An indicator of whether any part of the device was left in the subject's body after the device was removed, with identification of the part	Supplemental	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-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
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
F1121-C18559	C18559	Device implanted serious adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to serious device adverse effect(s) specification	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1121-C18564	C18564	Device log line number	The referenced line number of the entry on the device log	Supplemental	Devices 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.