CDE Catalog | NINDS Common Data Elements

***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

Subdisease Name

Subdomain Name

CRF Name

Displaying 57051 - 57075 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.
Select all	CDE ID	CDE Name	Definition	Classification	CRF Name	Disease Name	Subdisease Name
F0004-C60381	C60381	Serious adverse event investigator assessment reason other text	The free-text field related to 'Serious adverse event investigator assessment reason', specifying other text. Reason in the opinion of the principal investigator that is attributed as the cause of the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20404	C20404	Serious adverse event investigator assessment concurrent disorder specify text	The free-text field to specify the concurrent disorder 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)
F0004-C20403	C20403	Serious adverse event investigator assessment reason	Reason in the opinion of the principal investigator that is attributed as the cause of the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20413	C20413	Serious adverse event investigator assessment concomitant medication specify text	The free-text field to specify the concomitant medication 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)
F0004-C60380	C60380	Serious adverse event cause discontinue study indicator	Indicator of whether the serious adverse event caused the participant to be discontinued from the study	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20402	C20402	Study blind broken indicator	Indicator of whether the study blind was broken	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20400	C20400	Serious adverse event resolve end study intervention indicator	Indicator of whether a serious adverse event ended after the study intervention was stopped	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20401	C20401	Serious adverse event reappearance restart study intervention indicator	Indicator of whether the adverse event reappeared after the study intervention was restarted	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20399	C20399	Serious adverse event end study intervention indicator	Indicator of whether the study intervention was discontinued due to the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20398	C20398	Serious adverse event study intervention administration text	The free-text field to describe the administration of study intervention	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60379	C60379	Study intervention name	Name of study intervention	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20397	C20397	Serious adverse event relevant history text	The free-text field that describes relevant history including pre-existing medical conditions specific to the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20396	C20396	Serious adverse event concomitant medication text	The free-text field that describes the concomitant medications taken specific to the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20392	C20392	Serious adverse event treatment description text	The free-text field that describes the interventions specific to the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C20395	C20395	Serious adverse event laboratory data text	The free-text field that describes the relevant tests or laboratory data specific to the serious adverse event	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60378	C60378	Serious adverse event other important medical event text	The free-text field to describe the medically important event not covered by other 'serious' criteria	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60377	C60377	Serious adverse event other important medical event indicator	Indicator of whether the serious adverse event is a medically important event not covered by other 'serious' criteria	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60376	C60376	Serious adverse event associate congenital anomaly birth defect indicator	Indicator of whether the serious adverse event is associated with a congenital anomaly or birth defect	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60374	C60374	Serious adverse event intervention require prevent permanent impairment damage indicator	Indicator of whether the serious adverse event required intervention to prevent permanent impairment or damage	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60375	C60375	Serious adverse event result persistent significant disability incapacity indicator	Indicator of whether the serious adverse event resulted in persistent or significant disability or incapacity	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60373	C60373	Serious adverse event initial prolong hospital indicator	Indicator of whether the serious adverse event resulted in initial or prolonged hospitalization for the participant	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60372	C60372	Serious adverse event threaten life indicator	Indicator of whether the serious adverse event is life threatening	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0004-C60371	C60371	Serious adverse event result death indicator	Indicator of whether the serious adverse event resulted in death	Supplemental	Serious Adverse Events	General (For all diseases)	General (For all diseases)
F0009-C02311	C02311	Adverse event MedDRA lowest level term code	Code that corresponds to the Medical Dictionary for Regulatory Activities (MedDRA) Lowest Level Term (LLT) for an adverse event	Supplemental	Adverse Events	General (For all diseases)	General (For all diseases)
F0009-C02311	C02311	Adverse event MedDRA lowest level term code	Code that corresponds to the Medical Dictionary for Regulatory Activities (MedDRA) Lowest Level Term (LLT) for an adverse event	Supplemental	Adverse Events	Spinal Cord Injury	Spinal Cord Injury

Displaying 57051 - 57075 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.