Eligibility Acute Lymphoblastic Leukemia NCT01523782

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged ≥ 55 years
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
newly diagnosed all without prior treatment
Description

all

Type de données

boolean

Alias
UMLS CUI [1]
C0023449
patient capable to receive polychemotherapy (who < 2)
Description

polychemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0013218
with or without meningeal disease
Description

meningeal leukemia

Type de données

boolean

Alias
UMLS CUI [1]
C0948840
signed informed consent forms
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
subscribed to social security insurance
Description

social security insurance

Type de données

boolean

Alias
UMLS CUI [1]
C0021682
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
all t(9;22) and/or bcr-abl positive
Description

all t(9;22) and/or bcr-abl positive

Type de données

boolean

Alias
UMLS CUI [1]
C0279592
UMLS CUI [2]
C2861580
general state incompatible with chemotherapy treatment (who>2)
Description

general state incompatible with chemotherapy treatment

Type de données

boolean

Alias
UMLS CUI [1]
C1298650
UMLS CUI [2]
C0392920
presenting with a general or visceral contraindication to intensive treatment
Description

contraindication

Type de données

boolean

Alias
UMLS CUI [1]
C1301624
patient with another cancer other than all
Description

malignancy

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
severe evolutive infection or hiv seropositive or active hepatitis related to b or c viral infection
Description

communicable disease

Type de données

boolean

Alias
UMLS CUI [1]
C0009450
prior treatment with l-asparaginase (irrespective of the form)
Description

l-asparaginase

Type de données

boolean

Alias
UMLS CUI [1]
C0003993
history of grade 3 transfusional incident (life threatening)
Description

transfusional incident

Type de données

boolean

Alias
UMLS CUI [1]
C0161840
presenting rare and/or dangerous anti-erythrocyte antibodies thus leading to the unavailable of a phenotype compatible red blood cells
Description

anti-erythrocyte antibodies

Type de données

boolean

Alias
UMLS CUI [1]
C1112584
included in another clinical trial during the last 4weeks.
Description

study subject participation status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Acute Lymphoblastic Leukemia NCT01523782

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
aged ≥ 55 years
boolean
C0001779 (UMLS CUI [1])
all
Item
newly diagnosed all without prior treatment
boolean
C0023449 (UMLS CUI [1])
polychemotherapy
Item
patient capable to receive polychemotherapy (who < 2)
boolean
C0013218 (UMLS CUI [1])
meningeal leukemia
Item
with or without meningeal disease
boolean
C0948840 (UMLS CUI [1])
informed consent
Item
signed informed consent forms
boolean
C0021430 (UMLS CUI [1])
social security insurance
Item
subscribed to social security insurance
boolean
C0021682 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
all t(9;22) and/or bcr-abl positive
Item
all t(9;22) and/or bcr-abl positive
boolean
C0279592 (UMLS CUI [1])
C2861580 (UMLS CUI [2])
general state incompatible with chemotherapy treatment
Item
general state incompatible with chemotherapy treatment (who>2)
boolean
C1298650 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
contraindication
Item
presenting with a general or visceral contraindication to intensive treatment
boolean
C1301624 (UMLS CUI [1])
malignancy
Item
patient with another cancer other than all
boolean
C0006826 (UMLS CUI [1])
communicable disease
Item
severe evolutive infection or hiv seropositive or active hepatitis related to b or c viral infection
boolean
C0009450 (UMLS CUI [1])
l-asparaginase
Item
prior treatment with l-asparaginase (irrespective of the form)
boolean
C0003993 (UMLS CUI [1])
transfusional incident
Item
history of grade 3 transfusional incident (life threatening)
boolean
C0161840 (UMLS CUI [1])
anti-erythrocyte antibodies
Item
presenting rare and/or dangerous anti-erythrocyte antibodies thus leading to the unavailable of a phenotype compatible red blood cells
boolean
C1112584 (UMLS CUI [1])
study subject participation status
Item
included in another clinical trial during the last 4weeks.
boolean
C2348568 (UMLS CUI [1])