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 151 - 175 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
C18955 Device implanted other text

The free-text field related to 'Device implanted type' specifying other text. The type of device used

Supplemental 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
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
C14517 Device manufacturer name

The company responsible for development of the device

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
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
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
C14527 Device discontinuation reason

The reason the subject discontinued use 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
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
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
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
C14520 Device stimulation target anatomic site

The target of stimulation the device acts upon (where the device lead is located)

Supplemental Devices 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 Devices Log Epilepsy Epilepsy
C14521 Device lead type

Type of insulated wires (leads) for the device implanted

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 Devices Log Epilepsy Epilepsy
C14522 Device lead contact count

The number of contacts of the insulated wires (leads)

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
C02494 Imaging study date and time

Date (and time, if applicable and known) the radiologic study was obtained

Supplemental Functional Magnetic Resonance Imaging (fMRI) Epilepsy Epilepsy
C13968 Imaging functional magnetic resonance imaging analysis type

Types of functional magnetic resonance imaging (fMRI) analytic methods

Supplemental Functional Magnetic Resonance Imaging (fMRI) Epilepsy Epilepsy
C18893 Imaging perfusion technique other text

The free-text field related to 'Imaging perfusion technique type' specifying other text. Method of perfusion for imaging

Supplemental Functional Magnetic Resonance Imaging (fMRI) Epilepsy Epilepsy
C02495 Imaging scanner strength value type

Type of value, in Tesla (T), of the scanner's magnetic field strength used for the scan being reported

Supplemental Functional Magnetic Resonance Imaging (fMRI) Epilepsy Epilepsy
C13970 Brain region of interest type

Region of interest in the brain

Supplemental Functional Magnetic Resonance Imaging (fMRI) Epilepsy Epilepsy
C18894 Imaging functional magnetic resonance imaging analysis other text

The free-text field related to 'Imaging functional magnetic resonance imaging analysis type' specifying other text. Types of functional magnetic resonance imaging (fMRI) analytic methods

Supplemental Functional Magnetic Resonance Imaging (fMRI) Epilepsy Epilepsy
Displaying 151 - 175 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.