Eligibility AML NCT00079482

  1. StudyEvent: Eligibility
    1. Eligibility AML NCT00079482
Einschlusskriterien
Beskrivning

Einschlusskriterien

Alias
UMLS CUI-1
C1512693
AML
Beskrivning

AML

Datatyp

boolean

Alias
UMLS CUI-1
C0023467
Relapse
Beskrivning

Relapse

Datatyp

boolean

Alias
UMLS CUI-1
C0277556
FLT3 mutation
Beskrivning

FLT3 mutation

Datatyp

boolean

Alias
UMLS CUI-1
C2348501
Age
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI-1
C0001779
Life expectancy
Beskrivning

Life expectancy

Datatyp

boolean

Alias
UMLS CUI-1
C0023671
ECOG
Beskrivning

ECOG

Datatyp

boolean

Alias
UMLS CUI-1
C1828127
Not pregnant nor lactating
Beskrivning

Not pregnant nor lactating

Datatyp

boolean

Alias
UMLS CUI-1
C0232973
UMLS CUI-2
C1518422
UMLS CUI-3
C0006147
Ausschlusskriterien
Beskrivning

Ausschlusskriterien

Alias
UMLS CUI-1
C0680251
Bilirubin
Beskrivning

Bilirubin

Datatyp

boolean

Alias
UMLS CUI-1
C0201913
ALT and AST
Beskrivning

ALT and AST

Datatyp

boolean

Alias
UMLS CUI-1
C0001899
UMLS CUI-2
C0004002
Serum creatinine
Beskrivning

Serum creatinine

Datatyp

boolean

Alias
UMLS CUI-1
C0201976
Ejection fraction (EF)
Beskrivning

Ejection fraction (EF)

Datatyp

boolean

Alias
UMLS CUI-1
C0232174
Infection
Beskrivning

Infection

Datatyp

boolean

Alias
UMLS CUI-1
C0009450
Major physical or psychiatric condition
Beskrivning

Major physical or psychiatric condition

Datatyp

boolean

CNS involvement
Beskrivning

CNS involvement

Datatyp

boolean

Alias
UMLS CUI-1
C0449389
FLT3 inhibitor treatment
Beskrivning

FLT3 inhibitor treatment

Datatyp

boolean

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
CL414898
UMLS CUI-3
C1333568
HIV treatment
Beskrivning

HIV treatment

Datatyp

boolean

Alias
UMLS CUI-1
C0019693
Gastrointestinal ulceration or bleeding
Beskrivning

Gastrointestinal ulceration or bleeding

Datatyp

boolean

Alias
UMLS CUI-1
C0237938
UMLS CUI-2
C0017181
Other investigational drug
Beskrivning

Other investigational drug

Datatyp

boolean

Alias
UMLS CUI-1
C1516879

Similar models

Eligibility AML NCT00079482

  1. StudyEvent: Eligibility
    1. Eligibility AML NCT00079482
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Einschlusskriterien
C1512693 (UMLS CUI-1)
AML
Item
boolean
C0023467 (UMLS CUI-1)
Relapse
Item
boolean
C0277556 (UMLS CUI-1)
FLT3 mutation
Item
boolean
C2348501 (UMLS CUI-1)
Age
Item
boolean
C0001779 (UMLS CUI-1)
Life expectancy
Item
boolean
C0023671 (UMLS CUI-1)
ECOG
Item
boolean
C1828127 (UMLS CUI-1)
Not pregnant nor lactating
Item
boolean
C0232973 (UMLS CUI-1)
C1518422 (UMLS CUI-2)
C0006147 (UMLS CUI-3)
Item Group
Ausschlusskriterien
C0680251 (UMLS CUI-1)
Bilirubin
Item
boolean
C0201913 (UMLS CUI-1)
ALT and AST
Item
boolean
C0001899 (UMLS CUI-1)
C0004002 (UMLS CUI-2)
Serum creatinine
Item
boolean
C0201976 (UMLS CUI-1)
Ejection fraction (EF)
Item
boolean
C0232174 (UMLS CUI-1)
Infection
Item
boolean
C0009450 (UMLS CUI-1)
Major physical or psychiatric condition
Item
boolean
CNS involvement
Item
boolean
C0449389 (UMLS CUI-1)
FLT3 inhibitor treatment
Item
boolean
C0013227 (UMLS CUI-1)
CL414898 (UMLS CUI-2)
C1333568 (UMLS CUI-3)
HIV treatment
Item
boolean
C0019693 (UMLS CUI-1)
Gastrointestinal ulceration or bleeding
Item
boolean
C0237938 (UMLS CUI-1)
C0017181 (UMLS CUI-2)
Other investigational drug
Item
boolean
C1516879 (UMLS CUI-1)