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

CRF Name

Displaying 201 - 225 of 883

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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	Copyrighted or trademarked	Disease Name	Subdisease Name
F1115-C14546	C14546	EEG data original purpose type	The reason(s) for gathering data via electroencephalogram (EEG) method	Supplemental	Scalp Electroencephalography (EEG)	False	Epilepsy	Epilepsy
F1121-C14527	C14527	Device discontinuation reason	The reason the subject discontinued use of the device	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1120-C14514	C14514	Device implanted modification reason	The reason for modification of parameters or electrode configuration of original implanted device	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1120-C18559	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	Implanted Devices Log	False	Epilepsy	Epilepsy
F1121-C18559	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	False	Epilepsy	Epilepsy
F1122-C18559	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	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18558	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	Implanted Devices Log	False	Epilepsy	Epilepsy
F1121-C18558	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	False	Epilepsy	Epilepsy
F1122-C18558	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	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18556	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	False	Epilepsy	Epilepsy
F1121-C18556	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	False	Epilepsy	Epilepsy
F1122-C18556	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	False	Epilepsy	Epilepsy
F1122-C14534	C14534	Device implanted revision or replacement reason	The reason for device revision/replacement	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1123-C14357	C14357	Therapeutic brain stimulation pulse current value	The rate of flow of electrical charges through an electrode during stimulation pulses, measured in milliamperes, during a therapeutic brain stimulation procedure	Supplemental-Highly Recommended	Surgery and Pathology	False	Epilepsy	Epilepsy
F3064-C13973	C13973	Imaging epilepsy-specific protocol indicator	The protocol pertains to epilepsy	Supplemental	Magnetic Resonance Imaging (MRI)	False	Epilepsy	Epilepsy
F3064-C13979	C13979	Imaging abnormality feature type	The present abnormality feature(s)	Supplemental	Magnetic Resonance Imaging (MRI)	False	Epilepsy	Epilepsy
F1114-C13999	C13999	PET localization study type	The PET localization study conclusion	Supplemental	Positron Emission Tomography (PET) Localization	False	Epilepsy	Epilepsy
F1115-C18533	C18533	Electroencephalography ictal onset periodic discharge pattern type	The periodic discharge wave pattern of the brain on electroencephalogram (EEG) during onset of ictal discharge	Supplemental	Scalp Electroencephalography (EEG)	False	Epilepsy	Epilepsy
F1100-C00030	C00030	Race USA category	The patient's self declared racial origination, independent of ethnic origination, using OMB approved categories	Core	Demographics	False	Epilepsy	Epilepsy
F1807-C00030	C00030	Race USA category	The patient's self declared racial origination, independent of ethnic origination, using OMB approved categories	Core	General Core	False	Epilepsy	Epilepsy
F1107-C01521	C01521	Heart rate	The participant's pulse or number of contractions (heart beats) per minute	Supplemental	Vital Signs	False	Epilepsy	Epilepsy
F1123-C14347	C14347	Surgery radiosurgery marginal dose value	The numeric value measured for the dose of radiation (in Grays) delivered to the outer edge of the tumor	Supplemental-Highly Recommended	Surgery and Pathology	False	Epilepsy	Epilepsy
F1119-C18553	C18553	Medication non-anti-epileptic drug prior or concomitant use day count	The numeric count of days a non-anti-epileptic drug (NAED) was taken before or during a study	Supplemental	Non Anti Epileptic Medication Log	False	Epilepsy	Epilepsy
F1115-C14558	C14558	Seizures recorded only video count	The number of seizures with video ONLY, without electroencephalogram (EEG)	Supplemental	Scalp Electroencephalography (EEG)	False	Epilepsy	Epilepsy
F1115-C14557	C14557	Seizures recorded only EEG count	The number of seizures with electroencephalogram (EEG) only (without video)	Supplemental	Scalp Electroencephalography (EEG)	False	Epilepsy	Epilepsy

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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.