ID

44004

Beschreibung

Effects of Zometa and Physical Activity on Bone Density in Women Receiving Chemotherapy for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00202059

Link

https://clinicaltrials.gov/show/NCT00202059

Stichworte

  1. 09.07.16 09.07.16 -
  2. 20.09.21 20.09.21 -
Hochgeladen am

20. September 2021

DOI

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Lizenz

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT00202059

    Eligibility Breast Cancer NCT00202059

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    women with stage i - ii breast cancer
    Beschreibung

    Gender | Breast Carcinoma | TNM clinical staging

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2]
    C0678222
    UMLS CUI [3]
    C3258246
    ages 40 - 55
    Beschreibung

    Age

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    pre- or peri-menopausal
    Beschreibung

    Premenopausal state | Perimenopausal state

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0232969
    UMLS CUI [2]
    C3839366
    within 1 month of beginning adjuvant or neoadjuvant chemotherapy
    Beschreibung

    Adjuvant Chemotherapy Beginning | Neoadjuvant Chemotherapy Beginning

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0085533
    UMLS CUI [1,2]
    C0439659
    UMLS CUI [2,1]
    C0600558
    UMLS CUI [2,2]
    C0392920
    UMLS CUI [2,3]
    C0439659
    baseline lumbar spine and total hip bmd > -2.0 sd
    Beschreibung

    Bone Mineral Density Lumbar spine | Bone Mineral Density Entire hip region

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0005938
    UMLS CUI [1,2]
    C3887615
    UMLS CUI [2,1]
    C0005938
    UMLS CUI [2,2]
    C1281585
    able to read and write english
    Beschreibung

    English Language Able to read Able to write

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0376245
    UMLS CUI [1,2]
    C0586740
    UMLS CUI [1,3]
    C0584993
    signed consent form
    Beschreibung

    Informed consent

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    previous treatment with bisphosphonates
    Beschreibung

    Diphosphonates

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0012544
    laboratory evidence of renal disease
    Beschreibung

    Kidney Disease Evidence Laboratory

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0022658
    UMLS CUI [1,2]
    C3887511
    UMLS CUI [1,3]
    C0022885
    previous tram flap reconstructive surgery
    Beschreibung

    Breast reconstruction with TRAM flap

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1960508
    positive pregnancy test
    Beschreibung

    Pregnancy test positive

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0240802
    mental illness that precludes the patient from giving informed consent
    Beschreibung

    Mental disorders Exclusion Informed Consent

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0004936
    UMLS CUI [1,2]
    C2828389
    UMLS CUI [1,3]
    C0021430
    laboratory evidence of hepatic disease
    Beschreibung

    Liver disease Evidence Laboratory

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0023895
    UMLS CUI [1,2]
    C3887511
    UMLS CUI [1,3]
    C0022885

    Ähnliche Modelle

    Eligibility Breast Cancer NCT00202059

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Gender | Breast Carcinoma | TNM clinical staging
    Item
    women with stage i - ii breast cancer
    boolean
    C0079399 (UMLS CUI [1])
    C0678222 (UMLS CUI [2])
    C3258246 (UMLS CUI [3])
    Age
    Item
    ages 40 - 55
    boolean
    C0001779 (UMLS CUI [1])
    Premenopausal state | Perimenopausal state
    Item
    pre- or peri-menopausal
    boolean
    C0232969 (UMLS CUI [1])
    C3839366 (UMLS CUI [2])
    Adjuvant Chemotherapy Beginning | Neoadjuvant Chemotherapy Beginning
    Item
    within 1 month of beginning adjuvant or neoadjuvant chemotherapy
    boolean
    C0085533 (UMLS CUI [1,1])
    C0439659 (UMLS CUI [1,2])
    C0600558 (UMLS CUI [2,1])
    C0392920 (UMLS CUI [2,2])
    C0439659 (UMLS CUI [2,3])
    Bone Mineral Density Lumbar spine | Bone Mineral Density Entire hip region
    Item
    baseline lumbar spine and total hip bmd > -2.0 sd
    boolean
    C0005938 (UMLS CUI [1,1])
    C3887615 (UMLS CUI [1,2])
    C0005938 (UMLS CUI [2,1])
    C1281585 (UMLS CUI [2,2])
    English Language Able to read Able to write
    Item
    able to read and write english
    boolean
    C0376245 (UMLS CUI [1,1])
    C0586740 (UMLS CUI [1,2])
    C0584993 (UMLS CUI [1,3])
    Informed consent
    Item
    signed consent form
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Diphosphonates
    Item
    previous treatment with bisphosphonates
    boolean
    C0012544 (UMLS CUI [1])
    Kidney Disease Evidence Laboratory
    Item
    laboratory evidence of renal disease
    boolean
    C0022658 (UMLS CUI [1,1])
    C3887511 (UMLS CUI [1,2])
    C0022885 (UMLS CUI [1,3])
    Breast reconstruction with TRAM flap
    Item
    previous tram flap reconstructive surgery
    boolean
    C1960508 (UMLS CUI [1])
    Pregnancy test positive
    Item
    positive pregnancy test
    boolean
    C0240802 (UMLS CUI [1])
    Mental disorders Exclusion Informed Consent
    Item
    mental illness that precludes the patient from giving informed consent
    boolean
    C0004936 (UMLS CUI [1,1])
    C2828389 (UMLS CUI [1,2])
    C0021430 (UMLS CUI [1,3])
    Liver disease Evidence Laboratory
    Item
    laboratory evidence of hepatic disease
    boolean
    C0023895 (UMLS CUI [1,1])
    C3887511 (UMLS CUI [1,2])
    C0022885 (UMLS CUI [1,3])

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