ID

16552

Beschrijving

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

Trefwoorden

  1. 23-07-16 23-07-16 -
Geüploaded op

23 juli 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Leukemia NCT00022126

Eligibility Leukemia NCT00022126

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

Criteria

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

all or other leukemia

Datatype

boolean

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

cns or testicular disease allowed

Datatype

boolean

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

no l3 sig+ all or acute myelogenous leukemia

Datatype

boolean

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

gestation

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
patient characteristics:
Beschrijving

ID.5

Datatype

boolean

age:
Beschrijving

age

Datatype

boolean

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

diagnosis date

Datatype

boolean

Alias
UMLS CUI [1]
C2316983
performance status:
Beschrijving

performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1518965
not specified
Beschrijving

ID.9

Datatype

boolean

life expectancy:
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
not specified
Beschrijving

ID.11

Datatype

boolean

hematopoietic:
Beschrijving

hematopoietic

Datatype

boolean

Alias
UMLS CUI [1]
C0229601
not specified
Beschrijving

ID.13

Datatype

boolean

hepatic:
Beschrijving

hepatic

Datatype

boolean

Alias
UMLS CUI [1]
C0205054
not specified
Beschrijving

ID.15

Datatype

boolean

renal:
Beschrijving

renal

Datatype

boolean

Alias
UMLS CUI [1]
C0022646
not specified
Beschrijving

ID.17

Datatype

boolean

prior concurrent therapy:
Beschrijving

prior concurrent therapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514463
biologic therapy:
Beschrijving

biologic therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0005527
not specified
Beschrijving

ID.20

Datatype

boolean

chemotherapy:
Beschrijving

chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
not specified
Beschrijving

ID.22

Datatype

boolean

endocrine therapy:
Beschrijving

endocrine therapy

Datatype

boolean

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

steroid therapy

Datatype

boolean

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

chronic steroid treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0749016
radiotherapy:
Beschrijving

radiotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
not specified
Beschrijving

ID.27

Datatype

boolean

surgery:
Beschrijving

surgery

Datatype

boolean

Alias
UMLS CUI [1]
C0543467
not specified
Beschrijving

ID.29

Datatype

boolean

other:
Beschrijving

ID.30

Datatype

boolean

no other concurrent cytotoxic therapy
Beschrijving

no other concurrent cytotoxic therapy

Datatype

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)
Datatype
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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