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

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Operations

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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.
Select all	CDE ID	CDE Name	Definition	Classification	CRF Name	Copyrighted or trademarked	Disease Name	Subdisease Name
F0009-C60386	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	0	General (For all diseases)	General (For all diseases)
F0009-C60387	C60387	Adverse event ongoing indicator	Indicator of whether the adverse event experienced by the participant is ongoing	Supplemental	Adverse Events	0	General (For all diseases)	General (For all diseases)
F0009-C60388	C60388	Adverse event severity intensity CDISC grade	Grade of severity or intensity of the adverse event according to the Clinical Data Interchange Standards Consortium (CDISC) terminologies	Supplemental	Adverse Events	0	General (For all diseases)	General (For all diseases)
F0009-C60389	C60389	Adverse event study intervention action take type other text	The free-text field related to 'Adverse event study intervention action take type', specifying other text. Type of action taken for adverse event in relation to study intervention	Supplemental	Adverse Events	0	General (For all diseases)	General (For all diseases)
F0009-C60386	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	0	Spinal Cord Injury	Spinal Cord Injury
F0009-C60387	C60387	Adverse event ongoing indicator	Indicator of whether the adverse event experienced by the participant is ongoing	Supplemental	Adverse Events	0	Spinal Cord Injury	Spinal Cord Injury
F0009-C60388	C60388	Adverse event severity intensity CDISC grade	Grade of severity or intensity of the adverse event according to the Clinical Data Interchange Standards Consortium (CDISC) terminologies	Supplemental	Adverse Events	0	Spinal Cord Injury	Spinal Cord Injury
F0009-C60389	C60389	Adverse event study intervention action take type other text	The free-text field related to 'Adverse event study intervention action take type', specifying other text. Type of action taken for adverse event in relation to study intervention	Supplemental	Adverse Events	0	Spinal Cord Injury	Spinal Cord Injury
F0021-C60367	C60367	Autopsy indicator	Indicator of whether an autopsy was performed	Supplemental	Death Report	0	General (For all diseases)	General (For all diseases)
F0021-C60368	C60368	Death certificate status	Status of the participant's death certificate	Supplemental	Death Report	0	General (For all diseases)	General (For all diseases)
F1179-C60360	C60360	IV thrombolytic agent total dose	Dose of IV thrombolytic agent, in mg, given to the participant	Supplemental	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F1179-C60361	C60361	IV thrombolytic agent type	Type of IV thrombolytic agent given to the participant	Supplemental	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F1179-C60362	C60362	IV thrombolytic agent type other text	The free-text field related to 'IV thrombolytic agent type' specifying other text.	Supplemental	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F1179-C60363	C60363	IV thrombolytic agent not started reason	If NO Intravenous thrombolytic agent was initiated, documents reasons in the medical record for why no IV thrombolytic agent was started for the participant at the current hospital.	Supplemental	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F1179-C60364	C60364	IV thrombolytic agent not started other text	The free-text field related to 'IV thrombolytic agent not started reason' specifying other text. If NO Intravenous thrombolytic agent was initiated, documents reasons in the medical record for why no IV thrombolytic agent was started for the participant at the current hospital.	Supplemental	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F1179-C60365	C60365	IV thrombolytic agent not started MRI selection treatment beyond 4.5 hour reason	If NO Intravenous thrombolytic agent was initiated for the participant/subject treated using MRI imaging selection beyond 4.5 hours, documents reasons in the medical record for why no IV thrombolytic agent was started for the participant at the current hospital.	Exploratory	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F1179-C60366	C60366	IV thrombolytic agent at another hospital indicator	Indicator of whether IV thrombolytic agent was initiated for the participant at an outside hospital	Supplemental	Thrombolytic/Reperfusion Therapies	False	Stroke	Stroke
F0004-C60369	C60369	Serious adverse event site aware date and time	Date (and time, if applicable and known) on which the site first became aware of the serious adverse event	Supplemental	Serious Adverse Events	0	General (For all diseases)	General (For all diseases)
F0004-C60370	C60370	Serious adverse event ongoing indicator	Indicator of whether the serious adverse event experienced by the participant is ongoing	Supplemental	Serious Adverse Events	0	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	0	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	0	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	0	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	0	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	0	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	0	General (For all diseases)	General (For all diseases)

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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.