Common Data Element: Serious adverse event end treatment indicator
Listed below are the details for the data element.
1.0
Element Type
Common Data Element
Serious adverse event end treatment indicator
SerAdvrsEvntEndTxInd
Short Description
Indicate whether the study was discontinued due to the serious adverse event.
Definition
Indicate whether the study was discontinued due to the serious adverse event.
Biomedical Terminologies and Standards
Notes
Was study intervention discontinued due to the event?
Creation Date
2015-04-27
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
No instructions available
Preferred Question Text
Category Groups and Classifications
Disease | Domain | Sub-Domain |
---|---|---|
Epilepsy | Safety Data | Adverse Events |
General (For all diseases) | Safety Data | Adverse Events |
Classification
General (For all diseases)
:
Supplemental
Epilepsy
:
Supplemental
Keywords
Labels
Effective Date
Until Date
Last Change Date
Tue Apr 02 11:15:38 EDT 2024
See Also
AdvrsEvntDuringStudyInd;SeriousAdvrsEvntInd;SerAdvrsEvntAnticInd;SerAdvrsEvntCmntTxt;SerAdvrsEvntStartDateTime;SeradvrsEvntEndDateTime;SerAdvrsEvntOutcomStatus;InjElapsedTime
Submitting Organization Name
NIH/CIT/BRICS
Submitting Contact Name
Olga Vovk
Submitting Contact Information
olga.vovk@nih.gov
Steward Organization
Name
NIH/NINDS
Steward Contact Name
NINDSCDE
Steward Contact Information
NINDSCDE@emmes.com
NINDS ID