CDE Catalog

***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

Displaying 126 - 150 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.
CDE ID CDE Name Definition Classification CRF Name Copyrighted or trademarked Disease Name Subdisease Name
C18569 Device implanted new extension component model number

The model number of the new extension component

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C18578 Device implanted other revision component type

The modification of the other, unspecified component including explant, replacement, and repositioning

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C14534 Device implanted revision or replacement reason

The reason for device revision/replacement

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C18570 Device implanted new extension component registration number

The registration number of the new extension component

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C18579 Device implanted right extension revision component type

The modification of the right extension component including explant, replacement, and repositioning

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
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 Epilepsy Epilepsy
C18580 Device implanted right lead revision component type

The modification of the right lead component including explant, replacement, and repositioning

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C18582 Device revision replacement log line number

The referenced line number of the entry on the device revision replacment log

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C14515 Device implanted type

The type of device used

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
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 Epilepsy Epilepsy
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 Epilepsy Epilepsy
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 Epilepsy Epilepsy
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 Device Revision/Replacement Log Epilepsy Epilepsy
C18573 Device implanted new lead component model number

The model number of the new lead component

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C18960 Device implanted revision or replacement other text

The free-text field related to 'Device implanted revision or replacement reason' specifying other text. The reason for device revision/replacement

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C14530 Device implanted revision component type

The name of the components of the device that were modified or replaced

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
C18574 Device implanted new lead component registration number

The registration number of the new lead component

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C14531 Device implanted revision modification type

The modification of the components including explant, replacement, and repositioning

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
C18576 Device implanted other new component model number

The model number of the other, unspecified new component

Supplemental Device Revision/Replacement Log Epilepsy Epilepsy
C14524 Device permanent explant date

Date the device was removed from the subject

Supplemental Devices Log Epilepsy Epilepsy
C18956 Device stimulation target anatomic other text

The free-text field related to 'Device stimulation target anatomic site' specifying other text. The target of stimulation the device acts upon (where the device lead is located)

Supplemental Devices Log Epilepsy Epilepsy
Displaying 126 - 150 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.