ID

15757

Beschrijving

High-Dose Methotrexate (MTX) for Adult Acute Lymphoblastic Leukemia (ALL); ODM derived from: https://clinicaltrials.gov/show/NCT00131027

Link

https://clinicaltrials.gov/show/NCT00131027

Trefwoorden

  1. 11-06-16 11-06-16 -
Geüploaded op

11 juni 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Lymphoblastic Leukemia, Acute NCT00131027

Eligibility Lymphoblastic Leukemia, Acute NCT00131027

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
previously untreated bcr-abl-negative all
Beschrijving

bcr-abl-negative all

Datatype

boolean

Alias
UMLS CUI [1,1]
C0023449
UMLS CUI [1,2]
C1835417
age between 25 and 64 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
performance status between 0 and 3 (ecog criteria)
Beschrijving

performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
adequate functioning of the liver (serum bilirubin level < 2.0 mg/dl); kidneys (serum creatinine level < 2.0 mg/dl); and heart (left ventricular ejection fraction greater than 50% and no severe abnormalities detected on electrocardiograms and echocardiographs).
Beschrijving

liver renal and cardiac function

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0600061
UMLS CUI [3]
C0428772
written informed consent to participate in the trial
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
uncontrolled active infection
Beschrijving

active infection

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
another severe and/or life-threatening disease
Beschrijving

life-threatening disease

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
positive for hiv antibody and/or hepatitis b surface (hbs) antigen tests
Beschrijving

hiv antibody

Datatype

boolean

Alias
UMLS CUI [1]
C0019683
UMLS CUI [2]
C0019168
another primary malignancy which is clinically active and/or requires medical interventions
Beschrijving

another primary malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
pregnant and/or lactating women
Beschrijving

pregnancy or breast-feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
past history of renal failure
Beschrijving

history of renal failure

Datatype

boolean

Alias
UMLS CUI [1]
C0035078

Similar models

Eligibility Lymphoblastic Leukemia, Acute NCT00131027

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
bcr-abl-negative all
Item
previously untreated bcr-abl-negative all
boolean
C0023449 (UMLS CUI [1,1])
C1835417 (UMLS CUI [1,2])
age
Item
age between 25 and 64 years
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status between 0 and 3 (ecog criteria)
boolean
C1520224 (UMLS CUI [1])
liver renal and cardiac function
Item
adequate functioning of the liver (serum bilirubin level < 2.0 mg/dl); kidneys (serum creatinine level < 2.0 mg/dl); and heart (left ventricular ejection fraction greater than 50% and no severe abnormalities detected on electrocardiograms and echocardiographs).
boolean
C1278039 (UMLS CUI [1])
C0600061 (UMLS CUI [2])
C0428772 (UMLS CUI [3])
informed consent
Item
written informed consent to participate in the trial
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
active infection
Item
uncontrolled active infection
boolean
C0009450 (UMLS CUI [1])
life-threatening disease
Item
another severe and/or life-threatening disease
boolean
C0009488 (UMLS CUI [1])
hiv antibody
Item
positive for hiv antibody and/or hepatitis b surface (hbs) antigen tests
boolean
C0019683 (UMLS CUI [1])
C0019168 (UMLS CUI [2])
another primary malignancy
Item
another primary malignancy which is clinically active and/or requires medical interventions
boolean
C0006826 (UMLS CUI [1])
pregnancy or breast-feeding
Item
pregnant and/or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
history of renal failure
Item
past history of renal failure
boolean
C0035078 (UMLS CUI [1])

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