ID

16595

Beschrijving

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

Trefwoorden

  1. 08-12-15 08-12-15 -
  2. 25-07-16 25-07-16 -
Geüploaded op

25 juli 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

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

End of Study Psoriasis MIPSO EudraCT 2014-003022-40

End of Study
Beschrijving

End of Study

Alias
UMLS CUI-1
C0444496
Patient number
Beschrijving

Patient number

Datatype

text

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

Date end of study

Datatype

date

Alias
UMLS CUI [1]
C2983670
End of Study
Beschrijving

End of Study

Datatype

text

Alias
UMLS CUI [1]
C0444496
Early Study termination
Beschrijving

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

Datatype

integer

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

End of Study Reason

Datatype

text

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

Similar models

End of Study Psoriasis MIPSO EudraCT 2014-003022-40

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial