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End of Study AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

1 forms  
End of Study
Description

End of Study

End of Study Date
Description

End of Study Date

Data type

date

Alias
UMLS CUI-1
C2983670
Reason for End of Study
Description

Reason for End of Study

Data type

integer

Alias
UMLS CUI-1
C2348577
Specify if Reason for End of Study = 6 or 7
Description

Specify if Reason for End of Study = 6 or 7

Data type

text

Induction therapy I administrated
Description

Induction therapy I administrated

Data type

boolean

Alias
UMLS CUI-1
C0857127
UMLS CUI-2
C0205447
UMLS CUI-3
C1533734
Induction therapy II administrated
Description

Induction therapy II administrated

Data type

boolean

Alias
UMLS CUI-1
C0857127
UMLS CUI-2
C0205448
UMLS CUI-3
C1533734
Consolidation therapy I administrated
Description

Consolidation therapy I administrated

Data type

boolean

Alias
UMLS CUI-1
C1511484
UMLS CUI-2
C0205447
UMLS CUI-3
C1533734
Consolidation therapy II administrated
Description

Consolidation therapy II administrated

Data type

boolean

Alias
UMLS CUI-1
C1511484
UMLS CUI-2
C0205448
UMLS CUI-3
C1533734
Consolidation therapy III administrated
Description

Consolidation therapy III administrated

Data type

boolean

Alias
UMLS CUI-1
C1511484
UMLS CUI-2
C0205449
UMLS CUI-3
C1533734
Consolidation therapy IV administrated
Description

Consolidation therapy IV administrated

Data type

boolean

Alias
UMLS CUI-1
C1511484
UMLS CUI-2
C0205450
UMLS CUI-3
C1533734
Maintenance therapy administrated
Description

Maintenance therapy administrated

Data type

boolean

Alias
UMLS CUI-1
C0677908
UMLS CUI-2
C1533734
Signature
Description

Signature

Date
Description

Date

Data type

date

Alias
UMLS CUI-1
C0011008
Name of Investigator
Description

Name of Investigator

Data type

text

Alias
UMLS CUI-1
C2826892
Signature of investigator
Description

Signature of investigator

Data type

text

Alias
UMLS CUI-1
C2346576
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Similar models

End of Study AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
End of Study
End of Study Date
Item
End of Study Date
date
C2983670 (UMLS CUI-1)
Item
Reason for End of Study
integer
C2348577 (UMLS CUI-1)
Reason for End of Study
Code List
Reason for End of Study
CL Item
regular End of Study (0)
CL Item
no CR after Induction (1)
CL Item
exzessive extramedullary medical toxicity (2)
CL Item
dead (3)
CL Item
relapse after CR (4)
CL Item
Withdrawal of informed consent (5)
CL Item
Protocol deviation (6)
CL Item
other (7)
Specify if Reason for End of Study = 6 or 7
Item
Specify if Reason for End of Study = 6 or 7
text
Induction therapy I administrated
Item
Induction therapy I administrated
boolean
C0857127 (UMLS CUI-1)
C0205447 (UMLS CUI-2)
C1533734 (UMLS CUI-3)
Induction therapy II administrated
Item
Induction therapy II administrated
boolean
C0857127 (UMLS CUI-1)
C0205448 (UMLS CUI-2)
C1533734 (UMLS CUI-3)
Consolidation therapy I administrated
Item
Consolidation therapy I administrated
boolean
C1511484 (UMLS CUI-1)
C0205447 (UMLS CUI-2)
C1533734 (UMLS CUI-3)
Consolidation therapy II administrated
Item
Consolidation therapy II administrated
boolean
C1511484 (UMLS CUI-1)
C0205448 (UMLS CUI-2)
C1533734 (UMLS CUI-3)
Consolidation therapy III administrated
Item
Consolidation therapy III administrated
boolean
C1511484 (UMLS CUI-1)
C0205449 (UMLS CUI-2)
C1533734 (UMLS CUI-3)
Consolidation therapy IV administrated
Item
Consolidation therapy IV administrated
boolean
C1511484 (UMLS CUI-1)
C0205450 (UMLS CUI-2)
C1533734 (UMLS CUI-3)
Maintenance therapy administrated
Item
Maintenance therapy administrated
boolean
C0677908 (UMLS CUI-1)
C1533734 (UMLS CUI-2)
Item Group
Signature
Date
Item
Date
date
C0011008 (UMLS CUI-1)
Name of Investigator
Item
Name of Investigator
text
C2826892 (UMLS CUI-1)
Signature of investigator
Item
Signature of investigator
text
C2346576 (UMLS CUI-1)
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