ID

16012

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00193011

Palabras clave

  1. 2/5/16 2/5/16 -
  2. 26/6/16 26/6/16 -
Subido en

26 de junio de 2016

DOI

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Licencia

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT00193011

    Eligibility Breast Cancer NCT00193011

    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    to be included in this study, you must meet the following criteria:
    Descripción

    Inclusion criteria

    Tipo de datos

    boolean

    female patients with adenocarcinoma of the breast confirmed by biopsy
    Descripción

    female patients with adenocarcinoma of the breast

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0079399
    UMLS CUI [1,2]
    C0019638
    UMLS CUI [1,3]
    C0678222
    age 65 or older
    Descripción

    age

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    under age 65 must have significant medical illness, or general frailty
    Descripción

    significant medical illness

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0205082
    UMLS CUI [1,2]
    C0221423
    UMLS CUI [2]
    C0424594
    adequate bone marrow, liver or kidney function
    Descripción

    bone marrow, liver or kidney function

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0005953
    UMLS CUI [1,2]
    C0232741
    UMLS CUI [1,3]
    C0232804
    normal heart function
    Descripción

    cardiac function

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0232164
    less than 84 days from mastectomy/lumpectomy or axillary dissection
    Descripción

    time since surgery

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1272706
    UMLS CUI [1,2]
    C3714726
    signed consent obtained prior to initiation of any study procedures
    Descripción

    informed consent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    you cannot participate in this study if any of the following apply to you:
    Descripción

    Exclusion Criteria

    Tipo de datos

    boolean

    received neo-adjuvant therapy
    Descripción

    Neoadjuvant Therapy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0600558
    primary tumor is locally advanced at diagnosis
    Descripción

    locally advanced tumor

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0205179
    UMLS CUI [1,2]
    C0678222
    received prior chemotherapy within five years
    Descripción

    prior chemotherapy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1514457
    received previous radiation therapy within 5 years
    Descripción

    previous radiation therapy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    peripheral neuropathy
    Descripción

    Peripheral Neuropathy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0031117
    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.
    Descripción

    ID.15

    Tipo de datos

    boolean

    Similar models

    Eligibility Breast Cancer NCT00193011

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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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