ID

16595

Beskrivning

MIPSO Comparative study of bacterial microbiota in the skin and intestines of psoriasis patients before and after systemic treatment with adalimumab or ustekinumab or ciclosporin (EudraCT 2014-003022-40) Principal Investigator: Prof. Dr. Dr. H. C. Thomas A. Luger

Nyckelord

  1. 2015-12-08 2015-12-08 -
  2. 2016-07-25 2016-07-25 -
Uppladdad den

25 juli 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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End of Study Psoriasis MIPSO EudraCT 2014-003022-40 DRKS00007147

End of Study Psoriasis MIPSO EudraCT 2014-003022-40

End of Study
Beskrivning

End of Study

Alias
UMLS CUI-1
C0444496
Patient number
Beskrivning

Patient number

Datatyp

text

Alias
UMLS CUI [1]
C1830427
Date end of study
Beskrivning

Date end of study

Datatyp

date

Alias
UMLS CUI [1]
C2983670
End of Study
Beskrivning

End of Study

Datatyp

text

Alias
UMLS CUI [1]
C0444496
Early Study termination
Beskrivning

Early Study termination (if more than one, specify below)

Datatyp

integer

Alias
UMLS CUI [1]
C2718058
End of Study Reason
Beskrivning

End of Study Reason

Datatyp

text

Alias
UMLS CUI [1,1]
C0444496
UMLS CUI [1,2]
C0392360

Similar models

End of Study Psoriasis MIPSO EudraCT 2014-003022-40

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
End of Study
C0444496 (UMLS CUI-1)
Patient number
Item
text
C1830427 (UMLS CUI [1])
Date end of study
Item
date
C2983670 (UMLS CUI [1])
Item
text
C0444496 (UMLS CUI [1])
Code List
End of Study
CL Item
regular end of study (1)
CL Item
early study termination (2)
Item
Early Study termination
integer
C2718058 (UMLS CUI [1])
Code List
Early Study termination
CL Item
Change of treatment required (1)
CL Item
Patient's request (2)
CL Item
Inclusion/exclusion criteria were injured, before initializing therapy (3)
CL Item
Inclusion/exclusion criteria were injured, after initializing therapy (4)
CL Item
Entering pregnancy (5)
CL Item
Disallowed concomitant medication required (6)
CL Item
The continued participation in the clinical trial is medically no longer justifiable (7)
CL Item
Time windows for visits could not be complied with (8)
CL Item
Lack of patient compliance (9)
CL Item
Cancelation of the entire study (10)
CL Item
other reason (11)
End of Study Reason
Item
text
C0444496 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])

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