ID

13625

Description

AML96 - Risk-Adapted and Randomized Postremission-Therapy for Adult Acute Myeloid Leukemia Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00180115

Link

https://clinicaltrials.gov/show/NCT00180115

Keywords

Versions (1)
  1. 2/21/16 2/21/16 -
Uploaded on

February 21, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115

English

Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

AML of specific fab type

Data type

boolean

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

mds of specific fab type

Data type

boolean

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

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe comorbidities
Description

severe comorbidities

Data type

boolean

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

complications of the leukemia

Data type

boolean

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

prior therapy

Data type

boolean

Alias
UMLS CUI [1]
C1514463
hiv-infection
Description

hiv

Data type

boolean

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

allergy against study medication

Data type

boolean

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

pregnancy

Data type

boolean

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

missing written informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
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Similar models

Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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