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CDE Detailed Report
This report contains detailed information about the selected CDEs.
Note: If at least one CDE was selected from a copyright- or trademark-protected instrument/scale then all of the CDEs from that instrument/scale are included in this report.
Disease: Traumatic Brain Injury
SubDisease: Comprehensive
Sub-Domain: Off Treatment/Off Study
CRF: Study Discontinuation/Completion
Item count: 3 (3 distinct CDEs)
CDE ID
CDE Name
Variable Name
Definition / Description
Question Text
Permissible Value
Description
Data Type
Instructions
References
Population
Classification (e.g., Core)
Version #
Version Date
Aliases for Variable Name
CRF Module / Guideline
© or TM
Sub-Domain
Domain
Previous Title
Size
Input Restrictions
Min Value
Max Value
Measurement Type
LOINC ID
SNOMED
caDSR ID
CDISC ID
C02201
Off study intervention prematurely indicator
OffStdyIntrvntPrematureInd
Indicator that participant/subject discontinued study intervention before planned end of study
Indicates that participant/subject prematurely discontinued study intervention
Yes;No;Unknown;
Yes;No;Unknown;
Alphanumeric
Choose one.
No references available
Adult;Pediatric
Supplemental
3.0
7/20/2013
Aliases for variable name not defined
Study Discontinuation/Completion
Off Treatment/Off Study
Protocol Experience
Off study intervention prematurely indicator
 
Single Pre-Defined Value Selected
     
3180300
 
C18740
Off study intervention prematurely other text
OffStdyIntrvntPrematurOTH
The free-text field related to 'Off study intervention prematurely reason' specifying other text. Primary reason participant/subject discontinued study intervention before planned end of study
Other, specify
  
Alphanumeric
Choose all that apply.
No references available
Adult;Pediatric
Supplemental
1.0
5/27/2014
Aliases for variable name not defined
Study Discontinuation/Completion
Off Treatment/Off Study
Protocol Experience
 
4000
Free-Form Entry
     
2956831
 
C02222
Off study intervention prematurely reason
OffStdyIntrvntPrematurRsn
Primary reason participant/subject discontinued study intervention before planned end of study
Primary reason participant/subject prematurely discontinued study intervention
Adverse event;Other clinical decision (e.g., investigator decision, primary care provider decision, etc.) OR other reason specified by the protocol (i.e., institutionalization, pregnancy, etc.);Death;Participant's/Subject's decision (e.g., unwilling/unable to commit time and/or resources, moved from area, etc.);Lost to follow-up;Other, specify;
Adverse event;Other clinical decision (e.g., investigator decision, primary care provider decision, etc.) OR other reason specified by the protocol (i.e., institutionalization, pregnancy, etc.);Death;Participant's/Subject's decision (e.g., unwilling/unable to commit time and/or resources, moved from area, etc.);Lost to follow-up;Other, specify;
Alphanumeric
Choose all that apply.
No references available
Adult;Pediatric
Supplemental
3.0
7/20/2013
Aliases for variable name not defined
Study Discontinuation/Completion
Off Treatment/Off Study
Protocol Experience
Off study intervention prematurely reason
 
Single Pre-Defined Value Selected
     
2956831
 
12-11-2018
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