ID

15915

Descrição

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

Palavras-chave

  1. 06/06/2016 06/06/2016 -
  2. 18/06/2016 18/06/2016 -
Transferido a

18 de junho de 2016

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Childhood Acute Lymphoblastic Leukemia in Remission NCT00022737

Eligibility Childhood Acute Lymphoblastic Leukemia in Remission NCT00022737

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of acute lymphoblastic leukemia
Descrição

diagnosis of ALL

Tipo de dados

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
Descrição

prior front-line therapy on POG, CCG, COG study

Tipo de dados

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
Descrição

induction therapy

Tipo de dados

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:
Descrição

bone marrow status

Tipo de dados

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
Descrição

philadelphia chromosome translocation

Tipo de dados

boolean

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

bcr-abl fusion

Tipo de dados

boolean

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

hypodiploid

Tipo de dados

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
Descrição

mll translocation (11q23)

Tipo de dados

boolean

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

remission after induction therapy

Tipo de dados

boolean

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

m3 bone marrow status

Tipo de dados

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)
Descrição

m2 bone marrow status

Tipo de dados

boolean

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

ID.12

Tipo de dados

boolean

not pregnant or nursing
Descrição

pregnant or nursing

Tipo de dados

boolean

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

pregnancy test

Tipo de dados

boolean

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

contraception if fertile

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0700589
see disease characteristics
Descrição

ID.16

Tipo de dados

boolean

see disease characteristics
Descrição

ID.17

Tipo de dados

boolean

no concurrent prophylactic cranial radiotherapy
Descrição

concurrent prophylactic cranial radiotherapy

Tipo de dados

boolean

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

Similar models

Eligibility Childhood Acute Lymphoblastic Leukemia in Remission NCT00022737

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
diagnosis of ALL
Item
diagnosis of acute lymphoblastic leukemia
boolean
C0011900 (UMLS CUI [1,1])
C0023449 (UMLS CUI [1,2])
prior front-line therapy on POG, CCG, COG study
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])
induction therapy
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])
bone marrow status
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])
philadelphia chromosome translocation
Item
philadelphia chromosome positive (ph+) with t(9;22)(q34;q11) by cytogenetics or fluorescence in situ hybridization
boolean
C0856536 (UMLS CUI [1])
bcr-abl fusion
Item
bcr-abl fusion transcript by reverse transcription polymerase chain reaction
boolean
C1835417 (UMLS CUI [1])
hypodiploid
Item
hypodiploid with less than 44 chromosomes and/or dna index less than0.81
boolean
C1835417 (UMLS CUI [1])
C2919020 (UMLS CUI [2])
mll translocation (11q23)
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])
remission after induction therapy
Item
failed to achieve remission after front-line induction therapy
boolean
C0687702 (UMLS CUI [1])
m3 bone marrow status
Item
m3 bone marrow status (greater than 25% blasts) after induction therapy
boolean
C0678852 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
m2 bone marrow status
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
pregnant or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
pregnancy test
Item
negative pregnancy test
boolean
C0032976 (UMLS CUI [1])
contraception if fertile
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
concurrent prophylactic cranial radiotherapy
Item
no concurrent prophylactic cranial radiotherapy
boolean
C1522449 (UMLS CUI [1,1])
C3163632 (UMLS CUI [1,2])

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial