Informatie:
Fout:
ID
12649
Beschrijving
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
Trefwoorden
Versies (1)
- 07-12-15 07-12-15 -
Geüploaded op
7 december 2015
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Acute Lymphoblastic Leukaemia NCT01949129
Eligibility Acute Lymphoblastic Leukaemia NCT01949129
- StudyEvent: Eligibility
Similar models
Eligibility Acute Lymphoblastic Leukaemia NCT01949129
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])
C2347449 (UMLS CUI [2])
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])
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])
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])