ID

13138

Beschreibung

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

Stichworte

  1. 19.01.16 19.01.16 -
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CC BY-NC 3.0

Hochgeladen am

19. Januar 2016

DOI

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Creative Commons BY-NC 3.0

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Eligibility Acute Lymphocytic Leukemia NCT00773149

Eligibility Acute Lymphocytic Leukemia NCT00773149

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients older than 15 years
Beschreibung

age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
refractory all
Beschreibung

ALL

Datentyp

boolean

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

all in relapse post chemotherapy or post transplant

Datentyp

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.
Beschreibung

CD52

Datentyp

boolean

Alias
UMLS CUI [1]
C1267944
signed informed consent
Beschreibung

informed consent

Datentyp

boolean

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

social security coverage

Datentyp

boolean

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

contraception

Datentyp

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Beschreibung

Exclusion Criteria

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

children below 15 years of age or aged 15

Datentyp

boolean

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

blast cells not expressing cd52 antigen

Datentyp

boolean

Alias
UMLS CUI [1]
C1267944
hiv positivity
Beschreibung

HIV

Datentyp

boolean

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

ECOG score

Datentyp

boolean

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

hypersensitivity to alemtuzumab

Datentyp

boolean

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

pregnancy or breast feeding

Datentyp

boolean

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

malignancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826

Ähnliche Modelle

Eligibility Acute Lymphocytic Leukemia NCT00773149

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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