Eligibility AML NCT00079482

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

Einschlusskriterien

Alias
UMLS CUI-1
C1512693
AML
Descripción

AML

Tipo de datos

boolean

Alias
UMLS CUI-1
C0023467
Relapse
Descripción

Relapse

Tipo de datos

boolean

Alias
UMLS CUI-1
C0277556
FLT3 mutation
Descripción

FLT3 mutation

Tipo de datos

boolean

Alias
UMLS CUI-1
C2348501
Age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI-1
C0001779
Life expectancy
Descripción

Life expectancy

Tipo de datos

boolean

Alias
UMLS CUI-1
C0023671
ECOG
Descripción

ECOG

Tipo de datos

boolean

Alias
UMLS CUI-1
C1828127
Not pregnant nor lactating
Descripción

Not pregnant nor lactating

Tipo de datos

boolean

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

Ausschlusskriterien

Alias
UMLS CUI-1
C0680251
Bilirubin
Descripción

Bilirubin

Tipo de datos

boolean

Alias
UMLS CUI-1
C0201913
ALT and AST
Descripción

ALT and AST

Tipo de datos

boolean

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

Serum creatinine

Tipo de datos

boolean

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

Ejection fraction (EF)

Tipo de datos

boolean

Alias
UMLS CUI-1
C0232174
Infection
Descripción

Infection

Tipo de datos

boolean

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

Major physical or psychiatric condition

Tipo de datos

boolean

CNS involvement
Descripción

CNS involvement

Tipo de datos

boolean

Alias
UMLS CUI-1
C0449389
FLT3 inhibitor treatment
Descripción

FLT3 inhibitor treatment

Tipo de datos

boolean

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

HIV treatment

Tipo de datos

boolean

Alias
UMLS CUI-1
C0019693
Gastrointestinal ulceration or bleeding
Descripción

Gastrointestinal ulceration or bleeding

Tipo de datos

boolean

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

Other investigational drug

Tipo de datos

boolean

Alias
UMLS CUI-1
C1516879

Similar models

Eligibility AML NCT00079482

  1. StudyEvent: Eligibility
    1. Eligibility AML NCT00079482
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)