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 57026 - 57050 of 57153
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
C60386 Adverse event site aware date and time

Date (and time, if applicable and known) on which the site first became aware of the adverse event

Supplemental Adverse Events General (For all diseases) General (For all diseases)
C60386 Adverse event site aware date and time

Date (and time, if applicable and known) on which the site first became aware of the adverse event

Supplemental Adverse Events Spinal Cord Injury Spinal Cord Injury
C02306 Adverse event start date and time

Date (and time, if applicable and known) on which the adverse event was first evident

Supplemental Adverse Events General (For all diseases) General (For all diseases)
C02306 Adverse event start date and time

Date (and time, if applicable and known) on which the adverse event was first evident

Supplemental Adverse Events Spinal Cord Injury Spinal Cord Injury
C02306 Adverse event start date and time

Date (and time, if applicable and known) on which the adverse event was first evident

Supplemental Adverse Event Tracking Log Epilepsy Epilepsy
C02308 Adverse event during study indicator

Indicator of whether the participant experienced any adverse events during the study

Supplemental Adverse Events General (For all diseases) General (For all diseases)
C02308 Adverse event during study indicator

Indicator of whether the participant experienced any adverse events during the study

Supplemental Adverse Events Spinal Cord Injury Spinal Cord Injury
C02308 Adverse event during study indicator

Indicator of whether the participant experienced any adverse events during the study

Supplemental Adverse Event Tracking Log Epilepsy Epilepsy
C02308 Adverse event during study indicator

Indicator of whether the participant experienced any adverse events during the study

NeuroRehab Supplemental-Highly Recommended Assessments and Examinations Demographic and Clinical Conditions NeuroRehab NeuroRehab Comprehensive
C02308 Adverse event during study indicator

Indicator of whether the participant experienced any adverse events during the study

NeuroRehab Supplemental-Highly Recommended Assessments and Examinations Demographic and Clinical Conditions NeuroRehab NeuroRehab General
C20406 Serious adverse event comment text

The free-text field to provide any additional information that pertains to the serious adverse event

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C18659 Unexpected adverse event indicator

Indicator of whether the adverse event is unexpected

Supplemental Adverse Events General (For all diseases) General (For all diseases)
C18659 Unexpected adverse event indicator

Indicator of whether the adverse event is unexpected

Supplemental Adverse Events Spinal Cord Injury Spinal Cord Injury
C18659 Unexpected adverse event indicator

Indicator of whether the adverse event is unexpected

Supplemental Adverse Event Tracking Log Epilepsy Epilepsy
C18659 Unexpected adverse event indicator

Indicator of whether the adverse event is unexpected

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C20409 Adverse event sponsor attribution indicator

Indicator of whether the adverse event was caused by the study intervention in question, based on the sponsor's assessment

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C60385 Serious adverse event sponsor assessment indicator

Indicator of whether the adverse event is serious, based on the sponsor's assessment

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C20415 Serious adverse event report complete date

Date when the report on the serious adverse event was completed

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C20408 Serious adverse event report type

Type of report being completed for the serious adverse event

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C60384 Adverse event report identifier telephone number

Telephone number of an authorized group or person reporting the adverse event

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C20407 Adverse event report identifier name

Name of an authorized group or person reporting the adverse event

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C60383 Principal investigator address text

The free-text field to specify the principal investigator's address

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C60382 Principal investigator name

Name of principal investigator

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C20405 Serious adverse event anticipate indicator

Indicator of whether the serious adverse event was anticipated

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
C20414 Serious adverse event investigator assessment intervention withdrawal specify text

The free-text field to specify the details of the withdrawal of study intervention that might have caused the serious adverse event, in the opinion of the principal investigator

Supplemental Serious Adverse Events General (For all diseases) General (For all diseases)
Displaying 57026 - 57050 of 57153

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.