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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

  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

    Eligibility Acute Lymphoblastic Leukaemia NCT01949129

    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

    Similar models

    Eligibility Acute Lymphoblastic Leukaemia NCT01949129

    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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