ID

12795

Description

Therapy Protocol Acute Lymphoblastic Leukemia Stem Cell Transplantation International; ODM derived from: https://clinicaltrials.gov/show/NCT00861679

Link

https://clinicaltrials.gov/show/NCT00861679

Keywords

  1. 12/21/15 12/21/15 -
Uploaded on

December 21, 2015

DOI

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License

Creative Commons BY 4.0

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Eligibility Acute Lymphoblastic Leukemia NCT00861679

Eligibility Acute Lymphoblastic Leukemia NCT00861679

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients with all who fulfil the following criteria:
Description

all

Data type

boolean

Alias
UMLS CUI [1]
C0023449
age at time of initial diagnosis or relapse diagnosis, respectively ≤18 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
indication for allogeneic hsct
Description

allogeneic hsct

Data type

boolean

Alias
UMLS CUI [1]
C0472699
complete remission (cr) is achieved before sct
Description

complete remission before sct

Data type

boolean

Alias
UMLS CUI [1]
C0677874
UMLS CUI [2]
C1504389
written consent of the parents (legal guardian) and, if indicated, the minor patient via "informed consent form"
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
no pregnancy
Description

contraceptive methods

Data type

boolean

Alias
UMLS CUI [1]
C0700589
no secondary malignancy
Description

secondary malignancy

Data type

boolean

Alias
UMLS CUI [1]
C3266877
no previous hsct
Description

previous hsct

Data type

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C2242529
hsct is performed in a study participating centre.
Description

hsct is performed in a study participating centre

Data type

boolean

Alias
UMLS CUI [1]
C2827983
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with b-all
Description

b-all

Data type

text

Alias
UMLS CUI [1]
C0279593
informed consent not signed by parents (legal guardian)
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
pregnancy
Description

pregnant

Data type

boolean

Alias
UMLS CUI [1]
C0549206
secondary malignancy
Description

secondary malignancy

Data type

boolean

Alias
UMLS CUI [1]
C3266877
previous hsct
Description

previous hsct

Data type

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C2242529

Similar models

Eligibility Acute Lymphoblastic Leukemia NCT00861679

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
all
Item
all patients with all who fulfil the following criteria:
boolean
C0023449 (UMLS CUI [1])
age
Item
age at time of initial diagnosis or relapse diagnosis, respectively ≤18 years
boolean
C0001779 (UMLS CUI [1])
allogeneic hsct
Item
indication for allogeneic hsct
boolean
C0472699 (UMLS CUI [1])
complete remission before sct
Item
complete remission (cr) is achieved before sct
boolean
C0677874 (UMLS CUI [1])
C1504389 (UMLS CUI [2])
informed consent
Item
written consent of the parents (legal guardian) and, if indicated, the minor patient via "informed consent form"
boolean
C0021430 (UMLS CUI [1])
contraceptive methods
Item
no pregnancy
boolean
C0700589 (UMLS CUI [1])
secondary malignancy
Item
no secondary malignancy
boolean
C3266877 (UMLS CUI [1])
previous hsct
Item
no previous hsct
boolean
C0205156 (UMLS CUI [1,1])
C2242529 (UMLS CUI [1,2])
hsct is performed in a study participating centre
Item
hsct is performed in a study participating centre.
boolean
C2827983 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
b-all
Item
patients with b-all
text
C0279593 (UMLS CUI [1])
informed consent
Item
informed consent not signed by parents (legal guardian)
boolean
C0021430 (UMLS CUI [1])
pregnant
Item
pregnancy
boolean
C0549206 (UMLS CUI [1])
secondary malignancy
Item
secondary malignancy
boolean
C3266877 (UMLS CUI [1])
previous hsct
Item
previous hsct
boolean
C0205156 (UMLS CUI [1,1])
C2242529 (UMLS CUI [1,2])

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