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

Displaying 26 - 50 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
C56146 Assay result other text

The free-text field describing another result from the assay

Exploratory Biospecimens Collection and Processing Headache Headache
C16037 Pregnancy most recent live born infant indicator

Indicates whether the outcome of the participant/subject's most recent pregnancy was a live born infant?

Exploratory Pregnancy Outcome Headache Headache
C16051 Birth weight child value

Value of the weight of the participant/subject's child at birth

Exploratory Pregnancy Outcome Headache Headache
C16063 Pregnancy fetal diagnostic test date

Date the fetal diagnostic testing was performed during the pregnancy

Exploratory Pregnancy Outcome Headache Headache
C56140 Assay sensitivity specificity value

The value of the assay sensitivity and specificity

Exploratory Biospecimens Collection and Processing Headache Headache
C16064 Pregnancy fetal diagnostic test result

Results of the fetal diagnostic testing performed during the pregnancy

Exploratory Pregnancy Outcome Headache Headache
C18000 Congenital anomalies child specification text

Text specifying any congenital anomalies of the participant/subject

Exploratory Pregnancy Outcome Headache Headache
C56147 Headache free after specimen collection verified duration

The duration of time which the participant was verified to be headache-free after specimen collection

Exploratory Biospecimens Collection and Processing Headache Headache
C16040 Pregnancy fetus normal indicator

Indicates whether the fetus was normal

Exploratory Pregnancy Outcome Headache Headache
C16053 Birth length child value

Value of the length of the participant's/subject's child at birth

Exploratory Pregnancy Outcome Headache Headache
C16065 Congenital anomaly child indicator

Indicates whether there were congenital anomalies in the participant's/subject's child

Exploratory Pregnancy Outcome Headache Headache
C18001 Newborn complication child specification text

Text specifying other newborn complications

Exploratory Pregnancy Outcome Headache Headache
C56148 Headache type text

Text specifying the type of headache the participant/subject had, has, or is having

Exploratory Biospecimens Collection and Processing 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

Exploratory Pregnancy Outcome Headache Headache
C16042 Delivery mode induced reason

Type of induced delivery that occurred during the live infant birth

Exploratory Pregnancy Outcome Headache Headache
C16055 Full term delivery child indicator

Indicates whether the participant's/subject's child was delivered full-term

Exploratory Pregnancy Outcome Headache Headache
C12779 Test assay perform date

Date the confirmatory diagnostic test or assay was performed

Exploratory Biospecimens Collection and Processing Headache Headache
C16067 Newborn complication child indicator

Indicates whether there were other newborn complications experienced by the participant's/subject's child

Exploratory Pregnancy Outcome Headache Headache
C56141 Assay upper detection limit value

The value of the upper limit of detection of the assay

Exploratory Biospecimens Collection and Processing Headache Headache
C18002 Placenta umbilical cord abnormality specification text

Text describing placenta or umbilical cord abnormalities

Exploratory Pregnancy Outcome Headache Headache
C56149 Headache treatment type

The type of treatment for the participant's headache

Exploratory Biospecimens Collection and Processing Headache Headache
C10558 Delivery or pregnancy termination last date and time

Date (and time if applicable and known) the female participant/subject last delivered a pregnancy or the pregnancy terminated (e.g., miscarriage, abortion)

Exploratory Pregnancy Outcome Headache Headache
C16044 Delivery cesarean section reason

Reason for the Cesarean section

Exploratory Pregnancy Outcome Headache Headache
C16056 Gestational age child value

Time elapsed between the first day of the last normal menstrual period and the day the participant/subject delivered the neonate

Exploratory Pregnancy Outcome Headache Headache
C16069 Placenta umbilical cord abnormality indicator

Indicates whether the participant/subject experienced any abnormalities of placenta or umbilical cord

Exploratory Pregnancy Outcome Headache Headache
Displaying 26 - 50 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.