ID

14459

Description

Trial for Treatment of Adult Patients With Standard Risk Acute Lymphoblastic Leukemia With Chemotherapy and Rituximab; ODM derived from: https://clinicaltrials.gov/show/NCT00199004

Link

https://clinicaltrials.gov/show/NCT00199004

Keywords

  1. 4/16/16 4/16/16 -
Uploaded on

April 16, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Adult Acute Lymphocytic Leukemia NCT00199004

Eligibility Adult Acute Lymphocytic Leukemia NCT00199004

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
b-precursor all (common / pre b-all)
Description

Precursor B-cell lymphoblastic leukemia

Data type

boolean

Alias
UMLS CUI [1]
C1292769
standard risk
Description

standard risk

Data type

boolean

Alias
UMLS CUI [1]
C3641091
cd20 expression >20%
Description

cd20 expression

Data type

boolean

Alias
UMLS CUI [1]
C3278899
ph/bcr-abl negative
Description

ph/bcr-abl negative

Data type

boolean

Alias
UMLS CUI [1]
C2347493
age 15-65 years (55-65 if biologically younger)
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
written informed consent
Description

written informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe complications due to leukemia or secondary illnesses
Description

severe complications

Data type

boolean

Alias
UMLS CUI [1]
C0009566
late relapse of childhood all
Description

acute lymphocytic leukemia in relapse

Data type

boolean

Alias
UMLS CUI [1]
C2367454
cytostatic pretreatment
Description

Cytostatic chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C2609342
pregnancy
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
severe psychiatric illness or other circumstances which may compromise cooperation of the patient or informed consent
Description

psychiatric illness

Data type

boolean

Alias
UMLS CUI [1]
C0004936
known severe allergy to foreign proteins
Description

known severe allergy to foreign proteins

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C2230096

Similar models

Eligibility Adult Acute Lymphocytic Leukemia NCT00199004

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Precursor B-cell lymphoblastic leukemia
Item
b-precursor all (common / pre b-all)
boolean
C1292769 (UMLS CUI [1])
standard risk
Item
standard risk
boolean
C3641091 (UMLS CUI [1])
cd20 expression
Item
cd20 expression >20%
boolean
C3278899 (UMLS CUI [1])
ph/bcr-abl negative
Item
ph/bcr-abl negative
boolean
C2347493 (UMLS CUI [1])
Age
Item
age 15-65 years (55-65 if biologically younger)
boolean
C0001779 (UMLS CUI [1])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
severe complications
Item
severe complications due to leukemia or secondary illnesses
boolean
C0009566 (UMLS CUI [1])
acute lymphocytic leukemia in relapse
Item
late relapse of childhood all
boolean
C2367454 (UMLS CUI [1])
Cytostatic chemotherapy
Item
cytostatic pretreatment
boolean
C2609342 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
psychiatric illness
Item
severe psychiatric illness or other circumstances which may compromise cooperation of the patient or informed consent
boolean
C0004936 (UMLS CUI [1])
known severe allergy to foreign proteins
Item
known severe allergy to foreign proteins
boolean
C0020517 (UMLS CUI [1,1])
C2230096 (UMLS CUI [1,2])

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