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ID

14536

Description

Tandem Autologous- Nonmyeloablative Allogeneic Transplant for Newly Diagnosed Multiple Myeloma (Trapianto Tandem Autologo-Allogenico Non Mieloablativo Nel Mieloma Alla Diagnosi); ODM derived from: https://clinicaltrials.gov/show/NCT00702247

Link

https://clinicaltrials.gov/show/NCT00702247

Keywords

  1. 4/19/16 4/19/16 -
Uploaded on

April 19, 2016

DOI

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License

Creative Commons BY 4.0

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    Eligibility Multiple Myeloma NCT00702247

    Eligibility Multiple Myeloma NCT00702247

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    durie-salmon stage iia-iiib multiple myeloma
    Description

    Durie-salmon stage

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0278723
    UMLS CUI [2]
    C0278724
    age > 18 and ≤ 65 years
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    previously untreated myeloma
    Description

    Untreated myeloma

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0026764
    UMLS CUI [1,2]
    C0332155
    presence of a sibling (potential donor)
    Description

    Sibling

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0037047
    bilirubins < twice normal;alat and asat < four times normal
    Description

    Bilirubin, alat and asat

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1278039
    UMLS CUI [2]
    C0201836
    UMLS CUI [3]
    C0201899
    left ventricular ejection fraction > 40%
    Description

    Left ventricular ejection fraction

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0428772
    creatinine clearances > 40 ml/min
    Description

    Creatinine clearance

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0373595
    pulmonary dysfunction with diffusing capacity for carbon monoxide (dlco) > 40% and/or need for continuous oxygen supplementation
    Description

    Dlco, continuous oxygen supplementation

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1516251
    UMLS CUI [2]
    C4039841
    karnofsky performance status > 60%
    Description

    Karnofsky performance status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0206065
    patients must give written informed consent
    Description

    Informed consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    age > 65 years
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    previously treated myeloma
    Description

    Treated myeloma

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0026764
    UMLS CUI [1,2]
    C0332154
    absence of a sibling (genetic randomisation cannot be applied)
    Description

    Sibling

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0037047
    karnofsky performance status score < 60%
    Description

    Karnofsky performance status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0206065
    hiv-infection
    Description

    HIV-infection

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0019693
    pregnancy
    Description

    Pregnancy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    refusal to use contraceptive techniques during and for 12 months following treatment
    Description

    Contraception

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0700589
    patients unable to give written informed consent
    Description

    Unable to informed consent

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C1299582
    ps. informed consent is obtained from each patient according to the institutional review boards of the participating centers. the study is conducted according to the declaration of helsinki.
    Description

    Informed consent: specification

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C2348235

    Similar models

    Eligibility Multiple Myeloma NCT00702247

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Durie-salmon stage
    Item
    durie-salmon stage iia-iiib multiple myeloma
    boolean
    C0278723 (UMLS CUI [1])
    C0278724 (UMLS CUI [2])
    Age
    Item
    age > 18 and ≤ 65 years
    boolean
    C0001779 (UMLS CUI [1])
    Untreated myeloma
    Item
    previously untreated myeloma
    boolean
    C0026764 (UMLS CUI [1,1])
    C0332155 (UMLS CUI [1,2])
    Sibling
    Item
    presence of a sibling (potential donor)
    boolean
    C0037047 (UMLS CUI [1])
    Bilirubin, alat and asat
    Item
    bilirubins < twice normal;alat and asat < four times normal
    boolean
    C1278039 (UMLS CUI [1])
    C0201836 (UMLS CUI [2])
    C0201899 (UMLS CUI [3])
    Left ventricular ejection fraction
    Item
    left ventricular ejection fraction > 40%
    boolean
    C0428772 (UMLS CUI [1])
    Creatinine clearance
    Item
    creatinine clearances > 40 ml/min
    boolean
    C0373595 (UMLS CUI [1])
    Dlco, continuous oxygen supplementation
    Item
    pulmonary dysfunction with diffusing capacity for carbon monoxide (dlco) > 40% and/or need for continuous oxygen supplementation
    boolean
    C1516251 (UMLS CUI [1])
    C4039841 (UMLS CUI [2])
    Karnofsky performance status
    Item
    karnofsky performance status > 60%
    boolean
    C0206065 (UMLS CUI [1])
    Informed consent
    Item
    patients must give written informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Age
    Item
    age > 65 years
    boolean
    C0001779 (UMLS CUI [1])
    Treated myeloma
    Item
    previously treated myeloma
    boolean
    C0026764 (UMLS CUI [1,1])
    C0332154 (UMLS CUI [1,2])
    Sibling
    Item
    absence of a sibling (genetic randomisation cannot be applied)
    boolean
    C0037047 (UMLS CUI [1])
    Karnofsky performance status
    Item
    karnofsky performance status score < 60%
    boolean
    C0206065 (UMLS CUI [1])
    HIV-infection
    Item
    hiv-infection
    boolean
    C0019693 (UMLS CUI [1])
    Pregnancy
    Item
    pregnancy
    boolean
    C0032961 (UMLS CUI [1])
    Contraception
    Item
    refusal to use contraceptive techniques during and for 12 months following treatment
    boolean
    C0700589 (UMLS CUI [1])
    Unable to informed consent
    Item
    patients unable to give written informed consent
    boolean
    C0021430 (UMLS CUI [1,1])
    C1299582 (UMLS CUI [1,2])
    Informed consent: specification
    Item
    ps. informed consent is obtained from each patient according to the institutional review boards of the participating centers. the study is conducted according to the declaration of helsinki.
    boolean
    C0021430 (UMLS CUI [1,1])
    C2348235 (UMLS CUI [1,2])

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