Our website detected that you are using a browser (Internet Explorer) that we no longer support. Please use the following browsers instead: Chrome, Firefox, Edge, or Safari.

D

E

M

O

Build Version:13.1.0-41


Listed below are the details for the data element.

1.0
Element Type
Common Data Element
Medication prior or concomitant use indicator
MedctnPriorConcomUseInd
Short Description
Indicator of whether the participant/subject reported taking any medications during the time period relevant to the study protocol
Definition
Indicator of whether the participant/subject reported taking any medications during the time period relevant to the study protocol
 

Biomedical Terminologies and Standards

Notes
NINDS ID: C02002. caDSR: 2220500
Creation Date
2018-07-10
Historical Notes
References
No references available

Data Type
Alphanumeric
Input Restrictions
Single Pre-Defined Value Selected
Pre-Defined Values
Population
Adult and Pediatric
Guidelines/Instructions
Choose one. If this question is answered YES then at least one prior/concomitant medication record needs to be recorded. Do NOT record study medications taken (if study has a drug intervention) on this form. Refer to the Study Drug Dosing form instructions to record study medications.
Preferred Question Text
Did the participant/subject take any medications before or during the study
Category Groups and Classifications
DiseaseDomainSub-Domain
Stroke Disease/Injury Related Events Classification

Classification

Stroke :
Supplemental
Keywords
STROKE
Labels
Effective Date
Until Date
Last Change Date
Tue Jan 07 12:37:55 EST 2020
See Also
Submitting Organization Name
NIH/CIT/BRICS
Submitting Contact Name
Submitting Contact Information
Steward Organization Name
NIH/NINDS
Steward Contact Name
Steward Contact Information
NINDS ID

Change History