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 51 - 75 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
C18504 Cranial nerves abnormality present text

The free-text field to explain the abnormality of the cranial nerve identified

Supplemental Neurological Exam Epilepsy Epilepsy
C18932 Cranial nerves global assessment other text

The free-text field related to 'Cranial nerves global assessment result' specifying other text. The condition of Cranial Nerves

Supplemental Neurological Exam Epilepsy Epilepsy
C14433 Cranial nerves global assessment result

The condition of Cranial Nerves

Supplemental Neurological Exam Epilepsy Epilepsy
C06005 Data collected date and time

Date (and time, if applicable and known) the data were collected. This may be the date/time a particular examination or procedure was performed

Supplemental Neurological Exam Epilepsy Epilepsy
C06005 Data collected date and time

Date (and time, if applicable and known) the data were collected. This may be the date/time a particular examination or procedure was performed

Supplemental-Highly Recommended Classification of Seizures Epilepsy Epilepsy
C06005 Data collected date and time

Date (and time, if applicable and known) the data were collected. This may be the date/time a particular examination or procedure was performed

Supplemental-Highly Recommended Syndromes by Age of Onset Epilepsy Epilepsy
C14134 Data valid through date and time

Date (and time, if applicable and known) the data collected are valid through

Supplemental-Highly Recommended Syndromes by Age of Onset Epilepsy Epilepsy
C14134 Data valid through date and time

Date (and time, if applicable and known) the data collected are valid through

Supplemental-Highly Recommended Classification of Seizures Epilepsy Epilepsy
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 Epilepsy Epilepsy
C14518 Device component type

The name of a part of the device that has a registration number or serial number

Supplemental Devices Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
C14527 Device discontinuation reason

The reason the subject discontinued use of the device

Supplemental Devices Log Epilepsy Epilepsy
C14504 Device implanted amperage value

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

Supplemental Implanted Devices Log Epilepsy Epilepsy
C18555 Device implanted comment text

The free-text field to capture any comments related to an implanted device

Supplemental Implanted Devices Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
C14516 Device implanted implant date and time

Date (and time, if applicable and known) the device was implanted and became functional

Supplemental Devices 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 Implanted Devices 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 Devices 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
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
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 Epilepsy Epilepsy
C18557 Device implanted log line number

The reference line number of the entry on the implanted device log

Supplemental Implanted Devices Log Epilepsy Epilepsy
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 Epilepsy Epilepsy
C14514 Device implanted modification reason

The reason for modification of parameters or electrode configuration of original implanted device

Supplemental Implanted Devices Log Epilepsy Epilepsy
C14512 Device implanted negative electrode count

The number of negative electrodes used by the implanted device

Supplemental Implanted Devices Log Epilepsy Epilepsy
Displaying 51 - 75 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.