ID

16012

Beskrivning

Weekly Docetaxel and CMF in the Adjuvant Treatment of Elderly Women With High-Risk Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193011

Länk

https://clinicaltrials.gov/show/NCT00193011

Nyckelord

  1. 2016-05-02 2016-05-02 -
  2. 2016-06-26 2016-06-26 -
Uppladdad den

26 juni 2016

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT00193011

    Eligibility Breast Cancer NCT00193011

    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    to be included in this study, you must meet the following criteria:
    Beskrivning

    Inclusion criteria

    Datatyp

    boolean

    female patients with adenocarcinoma of the breast confirmed by biopsy
    Beskrivning

    female patients with adenocarcinoma of the breast

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0079399 (Gender)
    SNOMED
    263495000
    LOINC
    LP61312-2
    UMLS CUI [1,2]
    C0019638 (Histology)
    UMLS CUI [1,3]
    C0678222 (Breast Carcinoma)
    SNOMED
    254838004
    age 65 or older
    Beskrivning

    age

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    under age 65 must have significant medical illness, or general frailty
    Beskrivning

    significant medical illness

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0205082 (Severe (severity modifier))
    SNOMED
    24484000
    LOINC
    LA6750-9
    UMLS CUI [1,2]
    C0221423 (Illness (finding))
    SNOMED
    39104002
    UMLS CUI [2]
    C0424594 (Frailty)
    SNOMED
    248279007
    adequate bone marrow, liver or kidney function
    Beskrivning

    bone marrow, liver or kidney function

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0005953 (Bone Marrow)
    SNOMED
    279729006
    LOINC
    LP7410-6
    UMLS CUI [1,2]
    C0232741 (Liver function)
    SNOMED
    79036002
    LOINC
    LP31397-0
    UMLS CUI [1,3]
    C0232804 (Renal function)
    SNOMED
    11953005
    LOINC
    LP31398-8
    normal heart function
    Beskrivning

    cardiac function

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0232164 (Cardiac function)
    SNOMED
    86185002
    less than 84 days from mastectomy/lumpectomy or axillary dissection
    Beskrivning

    time since surgery

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1272706 (Interval)
    SNOMED
    385673002
    UMLS CUI [1,2]
    C3714726 (Operation on breast)
    SNOMED
    392090004
    signed consent obtained prior to initiation of any study procedures
    Beskrivning

    informed consent

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430 (Informed Consent)
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    you cannot participate in this study if any of the following apply to you:
    Beskrivning

    Exclusion Criteria

    Datatyp

    boolean

    received neo-adjuvant therapy
    Beskrivning

    Neoadjuvant Therapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0600558 (Neoadjuvant Therapy)
    primary tumor is locally advanced at diagnosis
    Beskrivning

    locally advanced tumor

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0205179 (Advanced phase)
    SNOMED
    86005002
    UMLS CUI [1,2]
    C0678222 (Breast Carcinoma)
    SNOMED
    254838004
    received prior chemotherapy within five years
    Beskrivning

    prior chemotherapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1514457 (Prior Chemotherapy)
    received previous radiation therapy within 5 years
    Beskrivning

    previous radiation therapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1522449 (Therapeutic radiology procedure)
    SNOMED
    53438000
    LOINC
    LA4351-8
    peripheral neuropathy
    Beskrivning

    Peripheral Neuropathy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0031117 (Peripheral Neuropathy)
    please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
    Beskrivning

    ID.15

    Datatyp

    boolean

    Similar models

    Eligibility Breast Cancer NCT00193011

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Inclusion criteria
    Item
    to be included in this study, you must meet the following criteria:
    boolean
    female patients with adenocarcinoma of the breast
    Item
    female patients with adenocarcinoma of the breast confirmed by biopsy
    boolean
    C0079399 (UMLS CUI [1,1])
    C0019638 (UMLS CUI [1,2])
    C0678222 (UMLS CUI [1,3])
    age
    Item
    age 65 or older
    boolean
    C0001779 (UMLS CUI [1])
    significant medical illness
    Item
    under age 65 must have significant medical illness, or general frailty
    boolean
    C0205082 (UMLS CUI [1,1])
    C0221423 (UMLS CUI [1,2])
    C0424594 (UMLS CUI [2])
    bone marrow, liver or kidney function
    Item
    adequate bone marrow, liver or kidney function
    boolean
    C0005953 (UMLS CUI [1,1])
    C0232741 (UMLS CUI [1,2])
    C0232804 (UMLS CUI [1,3])
    cardiac function
    Item
    normal heart function
    boolean
    C0232164 (UMLS CUI [1])
    time since surgery
    Item
    less than 84 days from mastectomy/lumpectomy or axillary dissection
    boolean
    C1272706 (UMLS CUI [1,1])
    C3714726 (UMLS CUI [1,2])
    informed consent
    Item
    signed consent obtained prior to initiation of any study procedures
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Exclusion Criteria
    Item
    you cannot participate in this study if any of the following apply to you:
    boolean
    Neoadjuvant Therapy
    Item
    received neo-adjuvant therapy
    boolean
    C0600558 (UMLS CUI [1])
    locally advanced tumor
    Item
    primary tumor is locally advanced at diagnosis
    boolean
    C0205179 (UMLS CUI [1,1])
    C0678222 (UMLS CUI [1,2])
    prior chemotherapy
    Item
    received prior chemotherapy within five years
    boolean
    C1514457 (UMLS CUI [1])
    previous radiation therapy
    Item
    received previous radiation therapy within 5 years
    boolean
    C1522449 (UMLS CUI [1])
    Peripheral Neuropathy
    Item
    peripheral neuropathy
    boolean
    C0031117 (UMLS CUI [1])
    ID.15
    Item
    please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
    boolean

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