ID

17852

Description

Dexamethasone Compared With Prednisone During Induction Therapy and Methotrexate With or Without Leucovorin During Maintenance Therapy in Treating Patients With Newly Diagnosed High-Risk Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00075725

Link

https://clinicaltrials.gov/show/NCT00075725

Keywords

Versions (2)
  1. 10/5/16 10/5/16 -
  2. 10/5/16 10/5/16 -
Uploaded on

October 5, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Leukemia NCT00075725

English

Eligibility Leukemia NCT00075725

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00075725
Criteria
Description

Criteria

newly diagnosed b-precursor acute lymphoblastic leukemia
Description

Precursor B-lymphoblastic leukaemia acute

Data type

boolean

Alias
UMLS CUI [1]
C1737235
wbc > 50,000/mm^3 for patients age 1 to 9
Description

White Blood Cell Count procedure | Age

Data type

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0001779
any wbc for patients age 10 to 30 or patients who have received prior steroid therapy or patients with testicular disease
Description

White Blood Cell Count procedure | Age | Steroid therapy | Testicular Disease

Data type

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0001779
UMLS CUI [3]
C0149783
UMLS CUI [4]
C0039584
must be eligible for and enrolled on classification study cog-aall03b1
Description

ALL Clinical Trial classification eligible | ALL Clinical Trial classification Enrollment

Data type

boolean

Alias
UMLS CUI [1,1]
C0023449
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0683326
UMLS CUI [1,4]
C1548635
UMLS CUI [2,1]
C0023449
UMLS CUI [2,2]
C0008976
UMLS CUI [2,3]
C0683326
UMLS CUI [2,4]
C1516879
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
1 to under 31
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
performance status
Description

performance status

Data type

boolean

Alias
UMLS CUI [1]
C1518965
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
life expectancy
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
hematopoietic
Description

Function Hematopoietic

Data type

boolean

Alias
UMLS CUI [1,1]
C0031843
UMLS CUI [1,2]
C0229601
see disease characteristics
Description

disease characteristic

Data type

boolean

Alias
UMLS CUI [1]
C0599878
hepatic
Description

Liver function

Data type

boolean

Alias
UMLS CUI [1]
C0232741
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
renal
Description

Renal function

Data type

boolean

Alias
UMLS CUI [1]
C0232804
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
prior concurrent therapy:
Description

Comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
biologic therapy
Description

Biological treatment

Data type

boolean

Alias
UMLS CUI [1]
C1531518
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
chemotherapy
Description

Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
no more than 72 hours since prior intrathecal cytarabine
Description

Cytarabine Intrathecal

Data type

boolean

Alias
UMLS CUI [1,1]
C0010711
UMLS CUI [1,2]
C0677897
no other prior cytotoxic chemotherapy
Description

Cytotoxic Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0677881
endocrine therapy
Description

Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279025
prior steroids allowed
Description

Steroids

Data type

boolean

Alias
UMLS CUI [1]
C0038317
radiotherapy
Description

Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C1522449
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
surgery
Description

Operative Surgical Procedures

Data type

boolean

Alias
UMLS CUI [1]
C0543467
not specified
Description

Unspecified

Data type

boolean

Alias
UMLS CUI [1]
C0205370
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Similar models

Eligibility Leukemia NCT00075725

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00075725
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Precursor B-lymphoblastic leukaemia acute
Item
newly diagnosed b-precursor acute lymphoblastic leukemia
boolean
C1737235 (UMLS CUI [1])
White Blood Cell Count procedure | Age
Item
wbc > 50,000/mm^3 for patients age 1 to 9
boolean
C0023508 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
White Blood Cell Count procedure | Age | Steroid therapy | Testicular Disease
Item
any wbc for patients age 10 to 30 or patients who have received prior steroid therapy or patients with testicular disease
boolean
C0023508 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0149783 (UMLS CUI [3])
C0039584 (UMLS CUI [4])
ALL Clinical Trial classification eligible | ALL Clinical Trial classification Enrollment
Item
must be eligible for and enrolled on classification study cog-aall03b1
boolean
C0023449 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0683326 (UMLS CUI [1,3])
C1548635 (UMLS CUI [1,4])
C0023449 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0683326 (UMLS CUI [2,3])
C1516879 (UMLS CUI [2,4])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Age
Item
1 to under 31
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status
boolean
C1518965 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Life Expectancy
Item
life expectancy
boolean
C0023671 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Function Hematopoietic
Item
hematopoietic
boolean
C0031843 (UMLS CUI [1,1])
C0229601 (UMLS CUI [1,2])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Liver function
Item
hepatic
boolean
C0232741 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Renal function
Item
renal
boolean
C0232804 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Comorbidity
Item
prior concurrent therapy:
boolean
C0009488 (UMLS CUI [1])
Biological treatment
Item
biologic therapy
boolean
C1531518 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Chemotherapy
Item
chemotherapy
boolean
C0392920 (UMLS CUI [1])
Cytarabine Intrathecal
Item
no more than 72 hours since prior intrathecal cytarabine
boolean
C0010711 (UMLS CUI [1,1])
C0677897 (UMLS CUI [1,2])
Cytotoxic Chemotherapy
Item
no other prior cytotoxic chemotherapy
boolean
C0677881 (UMLS CUI [1])
Hormone Therapy
Item
endocrine therapy
boolean
C0279025 (UMLS CUI [1])
Steroids
Item
prior steroids allowed
boolean
C0038317 (UMLS CUI [1])
Therapeutic radiology procedure
Item
radiotherapy
boolean
C1522449 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Operative Surgical Procedures
Item
surgery
boolean
C0543467 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
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