ID

14327

Description

Comparison of Different Combination Chemotherapy Regimens in Treating Infants With Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00015873

Link

https://clinicaltrials.gov/show/NCT00015873

Keywords

Versions (1)
  1. 4/11/16 4/11/16 -
Uploaded on

April 11, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Leukemia NCT00015873

English

Eligibility Leukemia NCT00015873

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00015873
Criteria
Description

Criteria

diagnosis of acute lymphoblastic leukemia (all)
Description

Acute lymphoblastic leukemia

Data type

boolean

Alias
UMLS CUI [1]
C0023449
newly diagnosed
Description

Date of diagnosis

Data type

boolean

Alias
UMLS CUI [1]
C2316983
morphological verification by cytochemistry and immunophenotyping
Description

Cytochemistry and immunophenotyping

Data type

boolean

Alias
UMLS CUI [1]
C0010741
UMLS CUI [2]
C0079611
cns or testicular leukemia at diagnosis allowed
Description

CNS or testicular leukemia

Data type

boolean

Alias
UMLS CUI [1]
C1332884
UMLS CUI [2]
C1336711
trisomy 21 allowed
Description

Trisomy 21

Data type

boolean

Alias
UMLS CUI [1]
C3537167
patient characteristics:
Description

Patient characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
age:
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
365 days or less
Description

Days

Data type

boolean

Alias
UMLS CUI [1]
C0439228
performance status:
Description

Performance status

Data type

boolean

Alias
UMLS CUI [1]
C1518965
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
life expectancy:
Description

Life expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
hematopoietic:
Description

Hematopoietic status

Data type

boolean

Alias
UMLS CUI [1]
C1292123
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
hepatic:
Description

Liver function

Data type

boolean

Alias
UMLS CUI [1]
C0232741
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
renal:
Description

Renal function

Data type

boolean

Alias
UMLS CUI [1]
C0232804
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
prior concurrent therapy:
Description

Concurrent therapy

Data type

boolean

Alias
UMLS CUI [1]
C0087111
biologic therapy:
Description

Biologic therapy

Data type

boolean

Alias
UMLS CUI [1]
C0005527
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
chemotherapy:
Description

Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
no prior chemotherapy for leukemia
Description

Prior chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1514457
endocrine therapy:
Description

Endocrine therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279025
at least 4 weeks since prior systemic corticosteroids
Description

Systemic corticosteroids

Data type

boolean

Alias
UMLS CUI [1]
C4039704
prior inhaled steroids allowed
Description

Inhaled steroids

Data type

boolean

Alias
UMLS CUI [1]
C2065041
radiotherapy:
Description

Radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1522449
no prior radiotherapy for leukemia
Description

Prior radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0279134
surgery:
Description

Surgery

Data type

boolean

Alias
UMLS CUI [1]
C0543467
not specified
Description

Specification

Data type

boolean

Alias
UMLS CUI [1]
C0205369
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Similar models

Eligibility Leukemia NCT00015873

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00015873
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Acute lymphoblastic leukemia
Item
diagnosis of acute lymphoblastic leukemia (all)
boolean
C0023449 (UMLS CUI [1])
Date of diagnosis
Item
newly diagnosed
boolean
C2316983 (UMLS CUI [1])
Cytochemistry and immunophenotyping
Item
morphological verification by cytochemistry and immunophenotyping
boolean
C0010741 (UMLS CUI [1])
C0079611 (UMLS CUI [2])
CNS or testicular leukemia
Item
cns or testicular leukemia at diagnosis allowed
boolean
C1332884 (UMLS CUI [1])
C1336711 (UMLS CUI [2])
Trisomy 21
Item
trisomy 21 allowed
boolean
C3537167 (UMLS CUI [1])
Patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Age
Item
age:
boolean
C0001779 (UMLS CUI [1])
Days
Item
365 days or less
boolean
C0439228 (UMLS CUI [1])
Performance status
Item
performance status:
boolean
C1518965 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
Life expectancy
Item
life expectancy:
boolean
C0023671 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
Hematopoietic status
Item
hematopoietic:
boolean
C1292123 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
Liver function
Item
hepatic:
boolean
C0232741 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
Renal function
Item
renal:
boolean
C0232804 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
Concurrent therapy
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Biologic therapy
Item
biologic therapy:
boolean
C0005527 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
Chemotherapy
Item
chemotherapy:
boolean
C0392920 (UMLS CUI [1])
Prior chemotherapy
Item
no prior chemotherapy for leukemia
boolean
C1514457 (UMLS CUI [1])
Endocrine therapy
Item
endocrine therapy:
boolean
C0279025 (UMLS CUI [1])
Systemic corticosteroids
Item
at least 4 weeks since prior systemic corticosteroids
boolean
C4039704 (UMLS CUI [1])
Inhaled steroids
Item
prior inhaled steroids allowed
boolean
C2065041 (UMLS CUI [1])
Radiotherapy
Item
radiotherapy:
boolean
C1522449 (UMLS CUI [1])
Prior radiotherapy
Item
no prior radiotherapy for leukemia
boolean
C0279134 (UMLS CUI [1])
Surgery
Item
surgery:
boolean
C0543467 (UMLS CUI [1])
Specification
Item
not specified
boolean
C0205369 (UMLS CUI [1])
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