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.

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Amyotrophic Lateral Sclerosis
Cerebral Palsy
Chiari I Malformation
Congenital Muscular Dystrophy
Duchenne Muscular Dystrophy/Becker Muscular Dystrophy
Epilepsy
Facioscapulohumeral Muscular Dystrophy
Friedreich's Ataxia
Frontotemporal Dementia
General (For all diseases)
Headache
Huntington's Disease
Mitochondrial Disease
Multiple Sclerosis
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
Myasthenia Gravis
Myotonic Muscular Dystrophy
NeuroRehab
Neuromuscular Diseases
Parkinson's Disease
Spinal Cord Injury
Spinal Muscular Atrophy
Sport-Related Concussion
Stroke
Traumatic Brain Injury
Unruptured Cerebral Aneurysms and Subarachnoid Hemorrhage
Displaying 426 - 450 of 1122
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
C15573 Imaging stimulation target type

The type of stimulation target of the imaging test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55774 Imaging headache relation time type

The type of timing of the imaging in relation to headache

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55775 Imaging ictal pain intensity value

The value related to the intensity of the subject's pain if the timing is ictal

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55776 Imaging ictal headache since onset duration

The duration of time since the onset of the subject's headache if it was ictal

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55777 Imaging inter peri ictal headache since end duration

The duration of time since the end of the subject's last inter-ictal or peri-ictal headahe

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55778 Imaging inter peri ictal next headache start duration

The duration of time until the start of the subject's next inter-ictal or peri-ictal headache

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55783 Imaging evoked potential (EV) laser nociceptive stimulation manufacturer name

The name of the laser nociceptive stimulation manufacturer used as part of the Blink Reflex and Evoked Potential Imaging test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55784 Imaging evoked potential (EV) laser nociceptive stimulation model name

The name of the laser nociceptive stimulation model used as part of the Blink Reflex and Evoked Potential Imaging test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55785 Imaging evoked potential (EV) Chemical nociceptive stimulation method name

The name of the chemical nociceptive stimulation method used as part of the Blink Reflex and Evoked Potential Imaging test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55786 Imaging evoked potential (EV) Chemical nociceptive stimulation substance name

The name of the chemical nociceptive stimulation substance used as part of the Blink Reflex and Evoked Potential Imaging test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55787 Imaging evoked potential (EV) recording parameter type

The type of recording parameter used for the imaging, as part of the Blink Reflex and Pain-Related Evoked Potentials Test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C55788 Imaging evoked potentials (EV) averaged response sequential block responses per block number

The number of sequential blocks of averaged responses and the number of responses in each block, as part of the Blink Reflex and Pain-Related Evoked Potentials Imaging test

 Supplemental Nociceptive Blink Reflex and Pain-Related Evoked Potentials False Headache Headache
C06005 Data collected date and time

Date (and time, if applicable and known) the data were collected. This may be the date/time a particular examination or procedure was performed

 Supplemental Pregnancy Information False Headache Headache
C10556 Pregnant ever indicator

Indicator as to whether or not the participant/subject has every been pregnant, both term and not to term

 Supplemental Pregnancy Information False Headache Headache
C10981 Birth control method type

The participant's method of birth control

 Supplemental Pregnancy Information False Headache Headache
C15624 Pregnancy indicator

Indicates if the participant/subject is currently pregnant

 Supplemental Pregnancy Information False Headache Headache
C16008 Birth control indicator

Indicates if participant uses birth control

 Supplemental Pregnancy Information False Headache Headache
C16009 Birth control last used date and time

Date (and time, if applicable and known) birth control was last used

 Supplemental Pregnancy Information False Headache Headache
C16011 Pregnancy confirmed date and time

Date the participant/subject's current pregnancy was confirmed

 Supplemental Pregnancy Information False Headache Headache
C16013 Pregnancy estimated delivery date ultrasound based indicator

Indicator of whether the estimated delivery date is based on an ultrasound examination

 Supplemental Pregnancy Information False Headache Headache
C16014 Pregnancy prenatal testing performed indicator

Indicator of whether prenatal testing was performed for the current pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16015 Prenatal testing type

The type of prenatal testing that was performed for the current pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16016 Prenatal testing date and time

Date the selected prenatal testing type was performed for the current pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16017 Prenatal testing result

Results of the selected prenatal testing type

 Supplemental Pregnancy Information False Headache Headache
C16018 Pregnancy complication indicator

Indicator of whether the participant/subject had complications during the pregnancy

 Supplemental Pregnancy Information False Headache Headache
Displaying 426 - 450 of 1122

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.