ID

13138

Description

Alemtuzumab (CAMPATH 1H) Associated to G-CSF in Adult Patients With Refractory Acute Lymphocytic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00773149

Link

https://clinicaltrials.gov/show/NCT00773149

Keywords

  1. 1/19/16 1/19/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 19, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Acute Lymphocytic Leukemia NCT00773149

Eligibility Acute Lymphocytic Leukemia NCT00773149

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients older than 15 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
refractory all
Description

ALL

Data type

boolean

Alias
UMLS CUI [1]
C0023449
all in relapse post chemotherapy or post transplant
Description

all in relapse post chemotherapy or post transplant

Data type

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C0472699
all blast cells expressing cd 52 antigen at any time during the evolution of the disease.
Description

CD52

Data type

boolean

Alias
UMLS CUI [1]
C1267944
signed informed consent
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patients under social security coverage
Description

social security coverage

Data type

boolean

Alias
UMLS CUI [1]
C0037435
anti conceptional tablets in pre menopausal women.
Description

contraception

Data type

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
children below 15 years of age or aged 15
Description

children below 15 years of age or aged 15

Data type

boolean

Alias
UMLS CUI [1]
C0001779
blast cells not expressing cd52 antigen (at all evaluations)
Description

blast cells not expressing cd52 antigen

Data type

boolean

Alias
UMLS CUI [1]
C1267944
hiv positivity
Description

HIV

Data type

boolean

Alias
UMLS CUI [1]
C0019682
ecog score 3 and 4
Description

ECOG score

Data type

boolean

Alias
UMLS CUI [1]
C1520224
hypersensitivity to alemtuzumab.
Description

hypersensitivity to alemtuzumab

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0383429
pregnancy or breast feeding.
Description

pregnancy or breast feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
other malignant disease in addition to all.
Description

malignancy

Data type

boolean

Alias
UMLS CUI [1]
C0006826

Similar models

Eligibility Acute Lymphocytic Leukemia NCT00773149

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
patients older than 15 years
boolean
C0001779 (UMLS CUI [1])
ALL
Item
refractory all
boolean
C0023449 (UMLS CUI [1])
all in relapse post chemotherapy or post transplant
Item
all in relapse post chemotherapy or post transplant
boolean
C0392920 (UMLS CUI [1])
C0472699 (UMLS CUI [2])
CD52
Item
all blast cells expressing cd 52 antigen at any time during the evolution of the disease.
boolean
C1267944 (UMLS CUI [1])
informed consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
social security coverage
Item
patients under social security coverage
boolean
C0037435 (UMLS CUI [1])
contraception
Item
anti conceptional tablets in pre menopausal women.
boolean
C0700589 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
children below 15 years of age or aged 15
Item
children below 15 years of age or aged 15
boolean
C0001779 (UMLS CUI [1])
blast cells not expressing cd52 antigen
Item
blast cells not expressing cd52 antigen (at all evaluations)
boolean
C1267944 (UMLS CUI [1])
HIV
Item
hiv positivity
boolean
C0019682 (UMLS CUI [1])
ECOG score
Item
ecog score 3 and 4
boolean
C1520224 (UMLS CUI [1])
hypersensitivity to alemtuzumab
Item
hypersensitivity to alemtuzumab.
boolean
C0020517 (UMLS CUI [1,1])
C0383429 (UMLS CUI [1,2])
pregnancy or breast feeding
Item
pregnancy or breast feeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
malignancy
Item
other malignant disease in addition to all.
boolean
C0006826 (UMLS CUI [1])

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