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

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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 451 - 475 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
C16020 Pregnancy infection illness indicator

Indicator of whether there were any infections/illnesses that occurred during this pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16022 Pregnancy prior history births full-term count

Count of the total number of pregnancies the participant/subject has carried for a full term (>= 37 weeks)

 Supplemental Pregnancy Information False Headache Headache
C16023 Pregnancy prior history births pre-term count

Count of the total number of pregnancies the participant/subject carried for less than a full term (

Supplemental Pregnancy Information False Headache Headache
C16024 Pregnancy prior history birth defect indicator

Indicator of whether a birth defect occurred in any of the participant/subject's previous pregnancies

 Supplemental Pregnancy Information False Headache Headache
C16026 Pregnancy prior history loss indicator

Indicator of whether a miscarriage ( 20 weeks) occurred in any previous pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16027 Pregnancy prior history loss week count

Number of the week of pregnancy during which the stillbirth or miscarriage occurred

 Supplemental Pregnancy Information False Headache Headache
C16028 Pregnancy prior history toxic exposure type

Type of any substances or radiation potentially harmful to the embryo or fetus to which the participant/subject has ever been exposed during pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16173 Pregnancy estimate delivery date and time

The date and time (if applicable) the participant is estimated to deliver the pregnancy

 Supplemental Pregnancy Information False Headache Headache
C16175 Menstrual period last date

Date of the participant's last menstrual period

 Supplemental Pregnancy Information False Headache Headache
C17993 Prenatal test text

Text notes of any comments regarding the selected prenatal testing type

 Supplemental Pregnancy Information False Headache Headache
C17994 Pregnancy complication text

Text specifying any complications the participant/subject experienced during this pregnancy

 Supplemental Pregnancy Information False Headache Headache
C17995 Pregnancy infection illness text

Text specifying any infections or illnesses the participant/subject experienced during this pregnancy

 Supplemental Pregnancy Information False Headache Headache
C17996 Pregnancy prior history birth defect text

Text of any comments about any birth defects that occurred during the participant/subject's previous pregnancies

 Supplemental Pregnancy Information False Headache Headache
C19040 Prenatal testing other text

The free-text field related to 'Prenatal testing type' specifying other text. The type of prenatal testing that was performed for the current pregnancy

 Supplemental Pregnancy Information False Headache Headache
C19044 Pregnancy prior history toxic exposure other text

The free-text field related to 'Pregnancy prior history toxic exposure type' specifying other text. Type of any substances or radiation potentially harmful to the embryo or fetus to which the participant/subject has ever been exposed during pregnancy

 Supplemental Pregnancy Information False Headache Headache
C55934 Pregnancy prior history births count

Count of the total number of pregnancies, either full-term or pre-term, that the patient/subject has been through

 Supplemental Pregnancy Information False Headache Headache
C02006 Medication prior or concomitant dose

Dose of prior/concomitant medication taken per administration

 Supplemental Rescue Treatments False Headache Headache
C02013 Medication prior or concomitant dose unit of measure UCUM code

Code that represents the dosage unit of measure of the prior or concomitant medication administered. Unified Code for Units of Measure (UCUM)

 Supplemental Rescue Treatments False Headache Headache
C02014 Medication prior or concomitant name

Name of the prior/concomitant agent or drug administered

 Supplemental Rescue Treatments False Headache Headache
C02015 Medication prior or concomitant route type

Type of access route for the administration of the prior/concomitant medication

 Supplemental Rescue Treatments False Headache Headache
C02016 Medication prior or concomitant start date and time

The date (and time, if applicable and known) on which the prior/concomitant medication usage began

 Supplemental Rescue Treatments False Headache Headache
C02025 Medication prior or concomitant RXNorm code

Code for name of the prior/concomitant agent or drug administered

 Supplemental Rescue Treatments False Headache Headache
C05122 Study therapy administered date and time

Date (and time, if applicable and known) the study therapy was administered to the participant/subject

 Supplemental Rescue Treatments False Headache Headache
C16211 Headache pain medication after study drug indicator

Indicator whether the subject has received any additional pain or headache medications after the study drug was administered

 Supplemental Rescue Treatments False Headache Headache
C18736 Medication prior or concomitant dose unit of measure other text

The free-text field related to 'Medication prior or concomitant dose unit of measure', specifying other text. Dosage unit of measure of the prior or concomitant medication administered

 Supplemental Rescue Treatments False Headache Headache
Displaying 451 - 475 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.