Eligibility Leukemia, Myeloid NCT00512083

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
primary refractory or relapsed aml
Description

Primary refractory or relapsed aml

Data type

boolean

Alias
UMLS CUI [1]
C0278780
confirmed diagnosis of aml (de novo or secondary) as defined by who classification
Description

Confirmed diagnosis aml

Data type

boolean

Alias
UMLS CUI [1,1]
C0023467
UMLS CUI [1,2]
C0011900
aged at least 18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
initial diagnosis of acute promyelocytic leukemia as defined by french-american-british criteria (bennett 1976)
Description

Acute Promyelocytic Leukemia

Data type

boolean

Alias
UMLS CUI [1]
C0023487
patient in blast crisis stage of chronic myeloid leukemia
Description

Blast crisis stage of chronic myeloid leukemia

Data type

boolean

Alias
UMLS CUI [1]
C0919644
received high-dose cytarabine (total cumulative dose of >6g/m sq)in last 6 months
Description

High-dose cytarabine

Data type

boolean

Alias
UMLS CUI [1]
C0010711
interval of <6 months between first onset of last complete remission and current relapse
Description

Interval first onset of last complete remission and current relapse

Data type

boolean

Alias
UMLS CUI [1,1]
C0677874
UMLS CUI [1,2]
C0035020
those with primary refractory leukemia who have received more than three previous induction cycles
Description

Primary refractory leukemia

Data type

boolean

Alias
UMLS CUI [1,1]
C0857127
UMLS CUI [1,2]
C0392920
relapsed patients who have received more than three previous treatment regimens
Description

Relapsed patients, more than three previous treatment regimens

Data type

boolean

Alias
UMLS CUI [1]
C0392920

Similar models

Eligibility Leukemia, Myeloid NCT00512083

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Primary refractory or relapsed aml
Item
primary refractory or relapsed aml
boolean
C0278780 (UMLS CUI [1])
Confirmed diagnosis aml
Item
confirmed diagnosis of aml (de novo or secondary) as defined by who classification
boolean
C0023467 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
Age
Item
aged at least 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute Promyelocytic Leukemia
Item
initial diagnosis of acute promyelocytic leukemia as defined by french-american-british criteria (bennett 1976)
boolean
C0023487 (UMLS CUI [1])
Blast crisis stage of chronic myeloid leukemia
Item
patient in blast crisis stage of chronic myeloid leukemia
boolean
C0919644 (UMLS CUI [1])
High-dose cytarabine
Item
received high-dose cytarabine (total cumulative dose of >6g/m sq)in last 6 months
boolean
C0010711 (UMLS CUI [1])
Interval first onset of last complete remission and current relapse
Item
interval of <6 months between first onset of last complete remission and current relapse
boolean
C0677874 (UMLS CUI [1,1])
C0035020 (UMLS CUI [1,2])
Primary refractory leukemia
Item
those with primary refractory leukemia who have received more than three previous induction cycles
boolean
C0857127 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Relapsed patients, more than three previous treatment regimens
Item
relapsed patients who have received more than three previous treatment regimens
boolean
C0392920 (UMLS CUI [1])