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 101 - 125 of 883
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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
C14531 Device implanted revision modification type

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

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
C14534 Device implanted revision or replacement reason

The reason for device revision/replacement

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
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
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 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 Devices 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
C14509 Device implanted stimulation off duration

Time in minutes of stimulation when the implanted device is off

Supplemental Implanted Devices Log Epilepsy Epilepsy
C14508 Device implanted stimulation on duration

Time in minutes of stimulation when the implanted device is on

Supplemental Implanted Devices Log Epilepsy Epilepsy
C14515 Device implanted type

The type of device used

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

The type of device used

Supplemental Devices Log Epilepsy Epilepsy
C14515 Device implanted type

The type of device used

Supplemental Implanted Devices Log Epilepsy Epilepsy
C14505 Device implanted voltage value

The electrical voltage as set in the implanted device (strength of the electric current)

Supplemental Implanted Devices Log Epilepsy Epilepsy
C14522 Device lead contact count

The number of contacts of the insulated wires (leads)

Supplemental Devices Log Epilepsy Epilepsy
C18957 Device lead other text

The free-text field related to 'Device lead type' specifying other text. Type of insulated wires (leads) for the device implanted

Supplemental Devices Log Epilepsy Epilepsy
C14521 Device lead type

Type of insulated wires (leads) for the device implanted

Supplemental Devices Log Epilepsy Epilepsy
C18564 Device log line number

The referenced line number of the entry on the device log

Supplemental Devices Log Epilepsy Epilepsy
C14517 Device manufacturer name

The company responsible for development of the device

Supplemental Devices Log Epilepsy Epilepsy
C18958 Device neurostimulator anatomic other text

The free-text field related to 'Device neurostimulator anatomic site' specifying other text. The location in the body of where the device is providing electrical stimulation

Supplemental Devices Log Epilepsy Epilepsy
C14523 Device neurostimulator anatomic site

The location in the body of where the device is providing electrical stimulation

Supplemental Devices Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
C14524 Device permanent explant date

Date the device was removed from the subject

Supplemental Devices 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
C14502 Device start date and time

Date (and time, if applicable and known) the device was functional and therapy was started with the parameters specified

Supplemental Implanted Devices Log Epilepsy Epilepsy
Displaying 101 - 125 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.