ID

30237

Description

NOPHO ALL-2008 Pilot Study on Consolidation Therapy for Children and Adolescents With Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00548431

Link

https://clinicaltrials.gov/show/NCT00548431

Keywords

  1. 5/23/18 5/23/18 -
  2. 5/23/18 5/23/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 23, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Leukemia, Lymphocytic, Acute NCT00548431

Eligibility Leukemia, Lymphocytic, Acute NCT00548431

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
b-lineage all
Description

Precursor B-cell lymphoblastic leukemia

Data type

boolean

Alias
UMLS CUI [1]
C1292769
1-17.9 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
wbc <100, clinical remission obtained day 2
Description

White Blood Cell Count procedure | Clinical Complete Response

Data type

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C4050094
written consent to participation.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
t(9;22)
Description

t(9;22)

Data type

boolean

Alias
UMLS CUI [1]
C3897138
hypodiploidy
Description

Hypoploidy

Data type

boolean

Alias
UMLS CUI [1]
C0333691
11q23-aberrations
Description

11q23 Aberration

Data type

boolean

Alias
UMLS CUI [1,1]
C0796367
UMLS CUI [1,2]
C0008625
tpmt-deficiency
Description

Thiopurine S methyltranferase deficiency

Data type

boolean

Alias
UMLS CUI [1]
C0342801
intolerance to mtx or 6mp
Description

Intolerance to Methotrexate | Intolerance to Mercaptopurine

Data type

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0025677
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0000618

Similar models

Eligibility Leukemia, Lymphocytic, Acute NCT00548431

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Precursor B-cell lymphoblastic leukemia
Item
b-lineage all
boolean
C1292769 (UMLS CUI [1])
Age
Item
1-17.9 years
boolean
C0001779 (UMLS CUI [1])
White Blood Cell Count procedure | Clinical Complete Response
Item
wbc <100, clinical remission obtained day 2
boolean
C0023508 (UMLS CUI [1])
C4050094 (UMLS CUI [2])
Informed Consent
Item
written consent to participation.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
t(9;22)
Item
t(9;22)
boolean
C3897138 (UMLS CUI [1])
Hypoploidy
Item
hypodiploidy
boolean
C0333691 (UMLS CUI [1])
11q23 Aberration
Item
11q23-aberrations
boolean
C0796367 (UMLS CUI [1,1])
C0008625 (UMLS CUI [1,2])
Thiopurine S methyltranferase deficiency
Item
tpmt-deficiency
boolean
C0342801 (UMLS CUI [1])
Intolerance to Methotrexate | Intolerance to Mercaptopurine
Item
intolerance to mtx or 6mp
boolean
C1744706 (UMLS CUI [1,1])
C0025677 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0000618 (UMLS CUI [2,2])

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