ID

19897

Descrição

The purpose of this study is to determine the safety and efficacy of natalizumab in the treatment of individuals who have been diagnosed with relapsing remitting multiple sclerosis (MS). It is hoped that natalizumab will prevent certain types of white blood cells from moving out of the bloodstream into organs, including the brain, that are being damaged by autoimmune disease (a disease in which the body's own immune system attacks certain organs). These white blood cells are thought to cause inflammation that can result in lesions (small areas of damage) in the brain. These lesions are thought to be the cause of relapses and disability in MS.

Palavras-chave

  1. 30/01/2017 30/01/2017 -
Transferido a

30 de janeiro de 2017

DOI

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Licença

Creative Commons BY-NC 3.0

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End of treatment CRFs Multiple Sklerosis Tysabri NCT00027300

End of treatment CRFs Multiple Sklerosis Tysabri NCT00027300

End of treatment
Descrição

End of treatment

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

Discontinue study drug prematurely

Tipo de dados

boolean

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

Reason

Tipo de dados

text

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

Reason study drug discontinued

Tipo de dados

integer

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

Reason description

Tipo de dados

text

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

Similar models

End of treatment CRFs Multiple Sklerosis Tysabri NCT00027300

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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])

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