End of treatment CRFs Multiple Sklerosis Tysabri NCT00027300

End of treatment
Beschrijving

End of treatment

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C0444930
Did the subject discontinue study drug prematurely?
Beschrijving

Discontinue study drug prematurely

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1444661
If "yes", mark the primary reason below
Beschrijving

Reason

Datatype

text

Alias
UMLS CUI [1]
C0392360
Reason, why subject discontinued study drug prematurely
Beschrijving

Reason study drug discontinued

Datatype

integer

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013216
UMLS CUI [1,3]
C1444662
Description:
Beschrijving

Reason description

Datatype

text

Alias
UMLS CUI [1,1]
C0678257
UMLS CUI [1,2]
C0392360

Similar models

End of treatment CRFs Multiple Sklerosis Tysabri NCT00027300

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
End of treatment
C0087111 (UMLS CUI-1)
C0444930 (UMLS CUI-2)
Discontinue study drug prematurely
Item
Did the subject discontinue study drug prematurely?
boolean
C0013227 (UMLS CUI [1,1])
C1444661 (UMLS CUI [1,2])
Reason
Item
If "yes", mark the primary reason below
text
C0392360 (UMLS CUI [1])
Item
Reason, why subject discontinued study drug prematurely
integer
C0392360 (UMLS CUI [1,1])
C0013216 (UMLS CUI [1,2])
C1444662 (UMLS CUI [1,3])
Code List
Reason, why subject discontinued study drug prematurely
CL Item
Lost to follow-up (describe below) (1 )
CL Item
Adverse event(s) (complete Adverse Event form) (2 )
CL Item
Voluntary withdrawal for reasons other than Adverse Event (describe below) (3 )
CL Item
Subject was non-compliant (4 )
CL Item
Death (complete Record of Death form) (5 )
CL Item
Other (describe below) (6 )
Reason description
Item
Description:
text
C0678257 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])