Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
de novo or secondary acute myeloid leukemia of the fab subtypes m0-m2 and m4-m7
Beschrijving

AML of specific fab type

Datatype

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2]
C0457321
de novo or secondary myelodysplastic syndrome fab subtypes raeb and raeb-t
Beschrijving

mds of specific fab type

Datatype

boolean

Alias
UMLS CUI [1]
C3463824
UMLS CUI [2]
C0457321
written informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe comorbidities
Beschrijving

severe comorbidities

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
severe uncontrolled complications of the leukemia
Beschrijving

complications of the leukemia

Datatype

boolean

Alias
UMLS CUI [1]
C0544688
previous therapy of leukemia/mds
Beschrijving

prior therapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514463
hiv-infection
Beschrijving

hiv

Datatype

boolean

Alias
UMLS CUI [1]
C0019682
known relevant allergy against study medication
Beschrijving

allergy against study medication

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1521826
pregnancy
Beschrijving

pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
missing written informed consent
Beschrijving

missing written informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
AML of specific fab type
Item
de novo or secondary acute myeloid leukemia of the fab subtypes m0-m2 and m4-m7
boolean
C0023467 (UMLS CUI [1])
C0457321 (UMLS CUI [2])
mds of specific fab type
Item
de novo or secondary myelodysplastic syndrome fab subtypes raeb and raeb-t
boolean
C3463824 (UMLS CUI [1])
C0457321 (UMLS CUI [2])
informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
severe comorbidities
Item
severe comorbidities
boolean
C0009488 (UMLS CUI [1])
complications of the leukemia
Item
severe uncontrolled complications of the leukemia
boolean
C0544688 (UMLS CUI [1])
prior therapy
Item
previous therapy of leukemia/mds
boolean
C1514463 (UMLS CUI [1])
hiv
Item
hiv-infection
boolean
C0019682 (UMLS CUI [1])
allergy against study medication
Item
known relevant allergy against study medication
boolean
C0020517 (UMLS CUI [1,1])
C1521826 (UMLS CUI [1,2])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
missing written informed consent
Item
missing written informed consent
boolean
C0021430 (UMLS CUI [1])