Eligibility Criteria

Inclusion and exclusion criteria
Beschreibung

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Confirmed diagnosis of newly diagnosed B-precursor acute lymphocytic leukemia
Beschreibung

Confirmed diagnosis of newly diagnosed B-precursor acute lymphocytic leukemia

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2585997
UMLS CUI [1,2]
C0750484
UMLS CUI [1,3]
C0349636
Participant is less than or equal to 21 years of age
Beschreibung

Participant is less than or equal to 21 years of age

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0001779
Written, informed consent following NCI, IRB, FDA, and OPRR Guidelines
Beschreibung

Written, informed consent following NCI, IRB, FDA, and OPRR Guidelines

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
Patient received high-dose methotrexate as part of protocol-directed therapy for ALL
Beschreibung

Patient received high-dose methotrexate as part of protocol-directed therapy for ALL

Datentyp

boolean

Alias
UMLS CUI [1,1]
C5204889
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0023449

Ähnliche Modelle

Eligibility Criteria

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Confirmed diagnosis of newly diagnosed B-precursor acute lymphocytic leukemia
Item
Confirmed diagnosis of newly diagnosed B-precursor acute lymphocytic leukemia
boolean
C2585997 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0349636 (UMLS CUI [1,3])
Participant is less than or equal to 21 years of age
Item
Participant is less than or equal to 21 years of age
boolean
C0001779 (UMLS CUI [1,1])
Written, informed consent following NCI, IRB, FDA, and OPRR Guidelines
Item
Written, informed consent following NCI, IRB, FDA, and OPRR Guidelines
boolean
C0021430 (UMLS CUI [1,1])
Patient received high-dose methotrexate as part of protocol-directed therapy for ALL
Item
Patient received high-dose methotrexate as part of protocol-directed therapy for ALL
boolean
C5204889 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0023449 (UMLS CUI [1,3])