ID

16552

Description

Combination Chemotherapy With or Without Donor Bone Marrow Transplantation in Treating Infants With Previously Untreated Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00022126

Link

https://clinicaltrials.gov/show/NCT00022126

Keywords

  1. 7/23/16 7/23/16 -
Uploaded on

July 23, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Leukemia NCT00022126

Eligibility Leukemia NCT00022126

  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00022126
Criteria
Description

Criteria

diagnosis of previously untreated acute lymphoblastic leukemia (all) or acute undifferentiated leukemia
Description

all or other leukemia

Data type

boolean

Alias
UMLS CUI [1]
C0023449
UMLS CUI [2]
C0280141
cns or testicular disease allowed
Description

cns or testicular disease allowed

Data type

boolean

Alias
UMLS CUI [1]
C0280141
UMLS CUI [2]
C0039584
no l3 sig+ all or acute myelogenous leukemia
Description

no l3 sig+ all or acute myelogenous leukemia

Data type

boolean

Alias
UMLS CUI [1]
C0279591
UMLS CUI [2]
C0023467
at least 36 weeks gestation for congenital all
Description

gestation

Data type

boolean

Alias
UMLS CUI [1]
C0032961
patient characteristics:
Description

ID.5

Data type

boolean

age:
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
under 366 days at diagnosis
Description

diagnosis date

Data type

boolean

Alias
UMLS CUI [1]
C2316983
performance status:
Description

performance status

Data type

boolean

Alias
UMLS CUI [1]
C1518965
not specified
Description

ID.9

Data type

boolean

life expectancy:
Description

life expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
not specified
Description

ID.11

Data type

boolean

hematopoietic:
Description

hematopoietic

Data type

boolean

Alias
UMLS CUI [1]
C0229601
not specified
Description

ID.13

Data type

boolean

hepatic:
Description

hepatic

Data type

boolean

Alias
UMLS CUI [1]
C0205054
not specified
Description

ID.15

Data type

boolean

renal:
Description

renal

Data type

boolean

Alias
UMLS CUI [1]
C0022646
not specified
Description

ID.17

Data type

boolean

prior concurrent therapy:
Description

prior concurrent therapy

Data type

boolean

Alias
UMLS CUI [1]
C1514463
biologic therapy:
Description

biologic therapy

Data type

boolean

Alias
UMLS CUI [1]
C0005527
not specified
Description

ID.20

Data type

boolean

chemotherapy:
Description

chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
not specified
Description

ID.22

Data type

boolean

endocrine therapy:
Description

endocrine therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279025
steroid therapy within 48 hours of study allowed if complete blood counts and lumbar puncture results known
Description

steroid therapy

Data type

boolean

Alias
UMLS CUI [1]
C0149783
no chronic steroid treatment for other disease
Description

chronic steroid treatment

Data type

boolean

Alias
UMLS CUI [1]
C0749016
radiotherapy:
Description

radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1522449
not specified
Description

ID.27

Data type

boolean

surgery:
Description

surgery

Data type

boolean

Alias
UMLS CUI [1]
C0543467
not specified
Description

ID.29

Data type

boolean

other:
Description

ID.30

Data type

boolean

no other concurrent cytotoxic therapy
Description

no other concurrent cytotoxic therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0009429

Similar models

Eligibility Leukemia NCT00022126

  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00022126
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
all or other leukemia
Item
diagnosis of previously untreated acute lymphoblastic leukemia (all) or acute undifferentiated leukemia
boolean
C0023449 (UMLS CUI [1])
C0280141 (UMLS CUI [2])
cns or testicular disease allowed
Item
cns or testicular disease allowed
boolean
C0280141 (UMLS CUI [1])
C0039584 (UMLS CUI [2])
no l3 sig+ all or acute myelogenous leukemia
Item
no l3 sig+ all or acute myelogenous leukemia
boolean
C0279591 (UMLS CUI [1])
C0023467 (UMLS CUI [2])
gestation
Item
at least 36 weeks gestation for congenital all
boolean
C0032961 (UMLS CUI [1])
ID.5
Item
patient characteristics:
boolean
age
Item
age:
boolean
C0001779 (UMLS CUI [1])
diagnosis date
Item
under 366 days at diagnosis
boolean
C2316983 (UMLS CUI [1])
performance status
Item
performance status:
boolean
C1518965 (UMLS CUI [1])
ID.9
Item
not specified
boolean
life expectancy
Item
life expectancy:
boolean
C0023671 (UMLS CUI [1])
ID.11
Item
not specified
boolean
hematopoietic
Item
hematopoietic:
boolean
C0229601 (UMLS CUI [1])
ID.13
Item
not specified
boolean
hepatic
Item
hepatic:
boolean
C0205054 (UMLS CUI [1])
ID.15
Item
not specified
boolean
renal
Item
renal:
boolean
C0022646 (UMLS CUI [1])
ID.17
Item
not specified
boolean
prior concurrent therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1])
biologic therapy
Item
biologic therapy:
boolean
C0005527 (UMLS CUI [1])
ID.20
Item
not specified
boolean
chemotherapy
Item
chemotherapy:
boolean
C0392920 (UMLS CUI [1])
ID.22
Item
not specified
boolean
endocrine therapy
Item
endocrine therapy:
boolean
C0279025 (UMLS CUI [1])
steroid therapy
Item
steroid therapy within 48 hours of study allowed if complete blood counts and lumbar puncture results known
boolean
C0149783 (UMLS CUI [1])
chronic steroid treatment
Item
no chronic steroid treatment for other disease
boolean
C0749016 (UMLS CUI [1])
radiotherapy
Item
radiotherapy:
boolean
C1522449 (UMLS CUI [1])
ID.27
Item
not specified
boolean
surgery
Item
surgery:
boolean
C0543467 (UMLS CUI [1])
ID.29
Item
not specified
boolean
ID.30
Item
other:
boolean
no other concurrent cytotoxic therapy
Item
no other concurrent cytotoxic therapy
boolean
C0392920 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])

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