ID

15633

Beschrijving

Combination Chemotherapy With or Without Peripheral Stem Cell Transplant in Treating Children With Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00022737

Link

https://clinicaltrials.gov/show/NCT00022737

Trefwoorden

  1. 06-06-16 06-06-16 -
  2. 18-06-16 18-06-16 -
Geüploaded op

6 juni 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Childhood Acute Lymphoblastic Leukemia in Remission NCT00022737

Eligibility Childhood Acute Lymphoblastic Leukemia in Remission NCT00022737

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of acute lymphoblastic leukemia
Beschrijving

ID.1

Datatype

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C0023449
received prior front-line therapy on a pediatric oncology group (pog),children's cancer group (ccg), or central oncology group (cog) study
Beschrijving

ID.2

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C1518932
received induction therapy comprising vincristine, asparaginase, prednisone/dexamethasone, and daunorubicin as in ccg, pog, or cog protocols
Beschrijving

ID.3

Datatype

boolean

Alias
UMLS CUI [1,1]
C3179010
UMLS CUI [1,2]
C0042679
UMLS CUI [2,1]
C3179010
UMLS CUI [2,2]
C0003993
UMLS CUI [3,1]
C3179010
UMLS CUI [3,2]
C0011777
UMLS CUI [4,1]
C3179010
UMLS CUI [4,2]
C3179010
UMLS CUI [5,1]
C3179010
UMLS CUI [5,2]
C0011015
m1 or m2 bone marrow status after front-line induction therapy and presenting with at least 1of the following:
Beschrijving

ID.4

Datatype

boolean

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0005953
philadelphia chromosome positive (ph+) with t(9;22)(q34;q11) by cytogenetics or fluorescence in situ hybridization
Beschrijving

ID.5

Datatype

boolean

Alias
UMLS CUI [1]
C0856536
bcr-abl fusion transcript by reverse transcription polymerase chain reaction
Beschrijving

ID.6

Datatype

boolean

Alias
UMLS CUI [1]
C1835417
hypodiploid with less than 44 chromosomes and/or dna index less than0.81
Beschrijving

ID.7

Datatype

boolean

Alias
UMLS CUI [1]
C1835417
UMLS CUI [2]
C2919020
mll translocation (11q23) by cytogenetics and a slow early response (ser) to induction therapy, defined as at least 5% blasts at day 15 of induction and/or at least .1% minimal residual disease (mrd) after induction therapy
Beschrijving

ID.8

Datatype

boolean

Alias
UMLS CUI [1,1]
C0796367
UMLS CUI [1,2]
C0796367
failed to achieve remission after front-line induction therapy
Beschrijving

ID.9

Datatype

boolean

Alias
UMLS CUI [1]
C0687702
m3 bone marrow status (greater than 25% blasts) after induction therapy
Beschrijving

ID.10

Datatype

boolean

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0005953
m2 bone marrow status (5-25% blasts) or at least 1% mrd after induction therapy and m2 or m3or at least 1% mrd after consolidation therapy (ccg studies) or extended induction therapy (pog or cog studies)
Beschrijving

ID.11

Datatype

boolean

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0005953
see disease characteristics
Beschrijving

ID.12

Datatype

boolean

not pregnant or nursing
Beschrijving

ID.13

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
negative pregnancy test
Beschrijving

ID.14

Datatype

boolean

Alias
UMLS CUI [1]
C0032976
fertile patients must use effective contraception
Beschrijving

ID.15

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
see disease characteristics
Beschrijving

ID.16

Datatype

boolean

see disease characteristics
Beschrijving

ID.17

Datatype

boolean

no concurrent prophylactic cranial radiotherapy
Beschrijving

ID.18

Datatype

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C3163632

Similar models

Eligibility Childhood Acute Lymphoblastic Leukemia in Remission NCT00022737

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosis of acute lymphoblastic leukemia
boolean
C0011900 (UMLS CUI [1,1])
C0023449 (UMLS CUI [1,2])
ID.2
Item
received prior front-line therapy on a pediatric oncology group (pog),children's cancer group (ccg), or central oncology group (cog) study
boolean
C1514463 (UMLS CUI [1,1])
C1518932 (UMLS CUI [1,2])
ID.3
Item
received induction therapy comprising vincristine, asparaginase, prednisone/dexamethasone, and daunorubicin as in ccg, pog, or cog protocols
boolean
C3179010 (UMLS CUI [1,1])
C0042679 (UMLS CUI [1,2])
C3179010 (UMLS CUI [2,1])
C0003993 (UMLS CUI [2,2])
C3179010 (UMLS CUI [3,1])
C0011777 (UMLS CUI [3,2])
C3179010 (UMLS CUI [4,1])
C3179010 (UMLS CUI [4,2])
C3179010 (UMLS CUI [5,1])
C0011015 (UMLS CUI [5,2])
ID.4
Item
m1 or m2 bone marrow status after front-line induction therapy and presenting with at least 1of the following:
boolean
C0678852 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
ID.5
Item
philadelphia chromosome positive (ph+) with t(9;22)(q34;q11) by cytogenetics or fluorescence in situ hybridization
boolean
C0856536 (UMLS CUI [1])
ID.6
Item
bcr-abl fusion transcript by reverse transcription polymerase chain reaction
boolean
C1835417 (UMLS CUI [1])
ID.7
Item
hypodiploid with less than 44 chromosomes and/or dna index less than0.81
boolean
C1835417 (UMLS CUI [1])
C2919020 (UMLS CUI [2])
ID.8
Item
mll translocation (11q23) by cytogenetics and a slow early response (ser) to induction therapy, defined as at least 5% blasts at day 15 of induction and/or at least .1% minimal residual disease (mrd) after induction therapy
boolean
C0796367 (UMLS CUI [1,1])
C0796367 (UMLS CUI [1,2])
ID.9
Item
failed to achieve remission after front-line induction therapy
boolean
C0687702 (UMLS CUI [1])
ID.10
Item
m3 bone marrow status (greater than 25% blasts) after induction therapy
boolean
C0678852 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
ID.11
Item
m2 bone marrow status (5-25% blasts) or at least 1% mrd after induction therapy and m2 or m3or at least 1% mrd after consolidation therapy (ccg studies) or extended induction therapy (pog or cog studies)
boolean
C0678852 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
ID.12
Item
see disease characteristics
boolean
ID.13
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.14
Item
negative pregnancy test
boolean
C0032976 (UMLS CUI [1])
ID.15
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1])
ID.16
Item
see disease characteristics
boolean
ID.17
Item
see disease characteristics
boolean
ID.18
Item
no concurrent prophylactic cranial radiotherapy
boolean
C1522449 (UMLS CUI [1,1])
C3163632 (UMLS CUI [1,2])

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