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ID

11850

Beskrivning

Epoetin Alfa Biosimilar in the Management of Chemotherapy-Induced Symptomatic Anemia in Haematology and Oncology; ODM derived from: https://clinicaltrials.gov/show/NCT02140736

Länk

https://clinicaltrials.gov/show/NCT02140736

Nyckelord

  1. 2015-08-10 2015-08-10 - Julian Varghese
Uppladdad den

10 augusti 2015

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility Chemotherapy-induced Symptomatic Anemia NCT02140736

    Eligibility Chemotherapy-induced Symptomatic Anemia NCT02140736

    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    patients of more than 18 years of age
    Beskrivning

    patients of more than 18 years of age

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    patients presenting with anemia following chemotherapy
    Beskrivning

    patients presenting with anemia following chemotherapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C3665472
    UMLS CUI [2]
    C0002871
    patients suffer from solid tumours, malignant hemopathies, lymphomas or myelomas and presenting with anemia following chemotherapy
    Beskrivning

    patients suffer from solid tumours, malignant hemopathies, lymphomas or myelomas and presenting with anemia following chemotherapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0280100
    UMLS CUI [2]
    C3665472
    UMLS CUI [3]
    C0376545
    - the patients may be included regardless of their chemotherapy cycle (from the first cycle until the last cycle)
    Beskrivning

    - the patients may be included regardless of their chemotherapy cycle (from the first cycle until the last cycle)

    Datatyp

    boolean

    patients eligible for epoetin alfa biosimilar treatment
    Beskrivning

    patients eligible for epoetin alfa biosimilar treatment

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0013893
    UMLS CUI [1,2]
    C0357126
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    patients are not receiving chemotherapy
    Beskrivning

    patients are not receiving chemotherapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C3665472
    patients already included in an epoetin zeta trial
    Beskrivning

    patients already included in an epoetin zeta trial

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C2242969
    UMLS CUI [1,2]
    C1997870
    patients presenting with a contraindication to epoetin zeta
    Beskrivning

    patients presenting with a contraindication to epoetin zeta

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0522473
    UMLS CUI [1,2]
    C1997870
    patients presenting with hypersensitivity to the active principle or any of the excipients
    Beskrivning

    patients presenting with hypersensitivity to the active principle or any of the excipients

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0020517
    UMLS CUI [1,2]
    C0014822
    patient with erythroblastopenia or acquired pure red cell aplasia (aprca)
    Beskrivning

    patient with erythroblastopenia or acquired pure red cell aplasia (aprca)

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0877221
    UMLS CUI [2]
    C0340961
    patient with uncontrollable arterial hypertension
    Beskrivning

    patient with uncontrollable arterial hypertension

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1868885
    patients who cannot receive adequate prophylaxis by antithrombotic agents
    Beskrivning

    patients who cannot receive adequate prophylaxis by antithrombotic agents

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0522473
    UMLS CUI [1,2]
    C1704311

    Similar models

    Eligibility Chemotherapy-induced Symptomatic Anemia NCT02140736

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    age
    Item
    patients of more than 18 years of age
    boolean
    C0001779 (UMLS CUI [1])
    Chemotherapy | Anemia | Hematologic Neoplasms
    Item
    patients presenting with anemia following chemotherapy
    boolean
    C3665472 (UMLS CUI [1])
    C0002871 (UMLS CUI [2])
    Solid tumour | Chemotherapy | Hematologic Neoplasms
    Item
    patients suffer from solid tumours, malignant hemopathies, lymphomas or myelomas and presenting with anemia following chemotherapy
    boolean
    C0280100 (UMLS CUI [1])
    C3665472 (UMLS CUI [2])
    C0376545 (UMLS CUI [3])
    patient inclusion regardless of chemotherapy
    Item
    - the patients may be included regardless of their chemotherapy cycle (from the first cycle until the last cycle)
    boolean
    Eligibility Determination; Epoetin Alfa
    Item
    patients eligible for epoetin alfa biosimilar treatment
    boolean
    C0013893 (UMLS CUI [1,1])
    C0357126 (UMLS CUI [1,2])
    Chemotherapy
    Item
    patients are not receiving chemotherapy
    boolean
    C3665472 (UMLS CUI [1])
    clinical trial participant (history); epoetin zeta
    Item
    patients already included in an epoetin zeta trial
    boolean
    C2242969 (UMLS CUI [1,1])
    C1997870 (UMLS CUI [1,2])
    Contraindication; epoetin zeta
    Item
    patients presenting with a contraindication to epoetin zeta
    boolean
    C0522473 (UMLS CUI [1,1])
    C1997870 (UMLS CUI [1,2])
    Hypersensitivity; Erythropoietin
    Item
    patients presenting with hypersensitivity to the active principle or any of the excipients
    boolean
    C0020517 (UMLS CUI [1,1])
    C0014822 (UMLS CUI [1,2])
    Decreased erythroid precursor production | Acquired red cell aplasia
    Item
    patient with erythroblastopenia or acquired pure red cell aplasia (aprca)
    boolean
    C0877221 (UMLS CUI [1])
    C0340961 (UMLS CUI [2])
    Uncontrolled hypertension
    Item
    patient with uncontrollable arterial hypertension
    boolean
    C1868885 (UMLS CUI [1])
    Contraindication; Antithrombotic Agents
    Item
    patients who cannot receive adequate prophylaxis by antithrombotic agents
    boolean
    C0522473 (UMLS CUI [1,1])
    C1704311 (UMLS CUI [1,2])

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