ID

16552

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00022126

Nyckelord

  1. 2016-07-23 2016-07-23 -
Uppladdad den

23 juli 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Leukemia NCT00022126

Eligibility Leukemia NCT00022126

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

Criteria

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

all or other leukemia

Datatyp

boolean

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

cns or testicular disease allowed

Datatyp

boolean

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

no l3 sig+ all or acute myelogenous leukemia

Datatyp

boolean

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

gestation

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
patient characteristics:
Beskrivning

ID.5

Datatyp

boolean

age:
Beskrivning

age

Datatyp

boolean

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

diagnosis date

Datatyp

boolean

Alias
UMLS CUI [1]
C2316983
performance status:
Beskrivning

performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1518965
not specified
Beskrivning

ID.9

Datatyp

boolean

life expectancy:
Beskrivning

life expectancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
not specified
Beskrivning

ID.11

Datatyp

boolean

hematopoietic:
Beskrivning

hematopoietic

Datatyp

boolean

Alias
UMLS CUI [1]
C0229601
not specified
Beskrivning

ID.13

Datatyp

boolean

hepatic:
Beskrivning

hepatic

Datatyp

boolean

Alias
UMLS CUI [1]
C0205054
not specified
Beskrivning

ID.15

Datatyp

boolean

renal:
Beskrivning

renal

Datatyp

boolean

Alias
UMLS CUI [1]
C0022646
not specified
Beskrivning

ID.17

Datatyp

boolean

prior concurrent therapy:
Beskrivning

prior concurrent therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C1514463
biologic therapy:
Beskrivning

biologic therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0005527
not specified
Beskrivning

ID.20

Datatyp

boolean

chemotherapy:
Beskrivning

chemotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0392920
not specified
Beskrivning

ID.22

Datatyp

boolean

endocrine therapy:
Beskrivning

endocrine therapy

Datatyp

boolean

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

steroid therapy

Datatyp

boolean

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

chronic steroid treatment

Datatyp

boolean

Alias
UMLS CUI [1]
C0749016
radiotherapy:
Beskrivning

radiotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C1522449
not specified
Beskrivning

ID.27

Datatyp

boolean

surgery:
Beskrivning

surgery

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
not specified
Beskrivning

ID.29

Datatyp

boolean

other:
Beskrivning

ID.30

Datatyp

boolean

no other concurrent cytotoxic therapy
Beskrivning

no other concurrent cytotoxic therapy

Datatyp

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
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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