ID

12649

Description

Allogeneic Stem Cell Transplantation for Children and Adolescents With Acute Lymphoblastic Leukaemia; ODM derived from: https://clinicaltrials.gov/show/NCT01949129

Link

https://clinicaltrials.gov/show/NCT01949129

Keywords

Versions (1)
  1. 12/7/15 12/7/15 -
Uploaded on

December 7, 2015

DOI

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License

Creative Commons BY 4.0
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Eligibility Acute Lymphoblastic Leukaemia NCT01949129

English

Eligibility Acute Lymphoblastic Leukaemia NCT01949129

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with all (except for patients with b-all) who fulfil the following criteria:
Description

patients with all

Data type

boolean

Alias
UMLS CUI [1]
C0027651
age at time of screening less than 18 years
Description

Age

Data type

boolean

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

indication for allogeneic hsct

Data type

boolean

Alias
UMLS CUI [1]
C0472699
complete remission (cr) before hsct
Description

complete remission (cr) before hsct

Data type

boolean

Alias
UMLS CUI [1,1]
C0677874
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C2242529
written consent of the parents (legal guardian) and, if necessary, the minor patient via "informed consent form"
Description

written consent of the parents (legal guardian) and, if necessary, the minor patient via "informed consent form"

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0030551
UMLS CUI [3]
C0026193
no pregnancy
Description

no pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0232973
no secondary malignancy
Description

no 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]
C0472699
UMLS CUI [2]
C2347449
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who do not fulfil the inclusion criteria
Description

patients who do not fulfil the inclusion criteria

Data type

boolean

Alias
UMLS CUI [1]
C1512693
non hodgkin-lymphoma
Description

non hodgkin-lymphoma

Data type

boolean

Alias
UMLS CUI [1]
C0024305
all with extramedullary involvement with indication for tbi
Description

all with extramedullary involvement with indication for tbi

Data type

boolean

Alias
UMLS CUI [1]
C1868812
cns involvement at the timepoint of screening
Description

cns involvement

Data type

boolean

Alias
UMLS CUI [1]
C0449389
trisomy 21
Description

trisomy 21

Data type

boolean

Alias
UMLS CUI [1]
C3537167
the whole protocol or essential parts are declined either by patient himself/herself or the respective legal guardian
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
no consent is given for saving and propagation of anonymous medical data for study reasons
Description

no consent is given for saving and propagation of anonymous medical data for study reasons

Data type

boolean

Alias
UMLS CUI [1]
C0021430
severe concomitant disease that does not allow treatment according to the protocol at the investigators discretion (e.g. malformation syndromes, cardiac malformations, metabolic disorders)
Description

severe concomitant disease that does not allow treatment according to the protocol at the investigator's discretion

Data type

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
karnofsky / lansky score < 50
Description

karnofsky / lansky score < 50

Data type

boolean

Alias
UMLS CUI [1]
C1522275
UMLS CUI [2]
C0206065
subjects unwilling or unable to comply with the study procedures
Description

subjects unwilling or unable to comply with the study procedures

Data type

boolean

Alias
UMLS CUI [1]
C1321605
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Similar models

Eligibility Acute Lymphoblastic Leukaemia NCT01949129

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
patients with all
Item
patients with all (except for patients with b-all) who fulfil the following criteria:
boolean
C0027651 (UMLS CUI [1])
Age
Item
age at time of screening less than 18 years
boolean
C0001779 (UMLS CUI [1])
indication for allogeneic hsct
Item
indication for allogeneic hsct
boolean
C0472699 (UMLS CUI [1])
complete remission (cr) before hsct
Item
complete remission (cr) before hsct
boolean
C0677874 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C2242529 (UMLS CUI [1,3])
written consent of the parents (legal guardian) and, if necessary, the minor patient via "informed consent form"
Item
written consent of the parents (legal guardian) and, if necessary, the minor patient via "informed consent form"
boolean
C0021430 (UMLS CUI [1])
C0030551 (UMLS CUI [2])
C0026193 (UMLS CUI [3])
no pregnancy
Item
no pregnancy
boolean
C0232973 (UMLS CUI [1])
no 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
C0472699 (UMLS CUI [1])
C2347449 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
patients who do not fulfil the inclusion criteria
Item
patients who do not fulfil the inclusion criteria
boolean
C1512693 (UMLS CUI [1])
non hodgkin-lymphoma
Item
non hodgkin-lymphoma
boolean
C0024305 (UMLS CUI [1])
all with extramedullary involvement with indication for tbi
Item
all with extramedullary involvement with indication for tbi
boolean
C1868812 (UMLS CUI [1])
cns involvement
Item
cns involvement at the timepoint of screening
boolean
C0449389 (UMLS CUI [1])
trisomy 21
Item
trisomy 21
boolean
C3537167 (UMLS CUI [1])
informed consent
Item
the whole protocol or essential parts are declined either by patient himself/herself or the respective legal guardian
boolean
C0021430 (UMLS CUI [1])
no consent is given for saving and propagation of anonymous medical data for study reasons
Item
no consent is given for saving and propagation of anonymous medical data for study reasons
boolean
C0021430 (UMLS CUI [1])
severe concomitant disease that does not allow treatment according to the protocol at the investigator's discretion
Item
severe concomitant disease that does not allow treatment according to the protocol at the investigators discretion (e.g. malformation syndromes, cardiac malformations, metabolic disorders)
boolean
C1321605 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
karnofsky / lansky score < 50
Item
karnofsky / lansky score < 50
boolean
C1522275 (UMLS CUI [1])
C0206065 (UMLS CUI [2])
subjects unwilling or unable to comply with the study procedures
Item
subjects unwilling or unable to comply with the study procedures
boolean
C1321605 (UMLS CUI [1])
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