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ID

13595

Beskrivning

Shorter Radiation Schedule for the Treatment of Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00201916

Länk

https://clinicaltrials.gov/show/NCT00201916

Nyckelord

  1. 2016-02-18 2016-02-18 -
Uppladdad den

18 februari 2016

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility Prostate Cancer NCT00201916

    Eligibility Prostate Cancer NCT00201916

    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    histologic diagnosis of adenocarcinoma of the prostate with no evidence of metastatic disease to the nodes, bone or lung
    Beskrivning

    prostate carcinoma, no metastases

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0600139
    UMLS CUI [2]
    C0027627
    stage t1a moderately or poorly differentiated, t1b, t1c or t2 by the current uicc-tnm classification
    Beskrivning

    tumor stage

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1300072
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    psa > 40 mcg/l
    Beskrivning

    psa

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0138741
    previous therapy for carcinoma of the prostate other than biopsy or turp, including patients previously on hormone therapy for treatment of their prostate cancer
    Beskrivning

    previous treatment

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0087111
    UMLS CUI [2]
    C0600139
    prior or active malignancy other than non-melanoma skin cancer; or colon or thyroid cancer treated a minimum of five years prior to study entry and presumed cured
    Beskrivning

    malignancies

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    simulated volume exceeds 1000 cm3
    Beskrivning

    tumor volume

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0475276
    previous pelvic radiotherapy
    Beskrivning

    previous pelvic radiotherapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1522449
    UMLS CUI [1,2]
    C0030797
    inflammatory bowel disease
    Beskrivning

    inflammatory bowel disease

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0021390
    serious non-malignant disease which would preclude radiotherapy or surgical biopsy
    Beskrivning

    comorbidity precluding radiotherapy or surgical biopsy

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    geographic inaccessibility for follow-up
    Beskrivning

    geographic inaccessibility for follow-up

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1321605
    psychiatric or addictive disorder which would preclude obtaining informed consent or adherence to protocol
    Beskrivning

    psychiatric or addictive disorder precluding consent or compliance

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    unable to commence radiation therapy within 26 weeks of the date of last prostatic biopsy
    Beskrivning

    unable to commence radiation therapy within 26 weeks

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1321605
    failure to give informed consent to participate in the study
    Beskrivning

    failure to give informed consent

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C0439801

    Similar models

    Eligibility Prostate Cancer NCT00201916

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    prostate carcinoma, no metastases
    Item
    histologic diagnosis of adenocarcinoma of the prostate with no evidence of metastatic disease to the nodes, bone or lung
    boolean
    C0600139 (UMLS CUI [1])
    C0027627 (UMLS CUI [2])
    tumor stage
    Item
    stage t1a moderately or poorly differentiated, t1b, t1c or t2 by the current uicc-tnm classification
    boolean
    C1300072 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    psa
    Item
    psa > 40 mcg/l
    boolean
    C0138741 (UMLS CUI [1])
    previous treatment
    Item
    previous therapy for carcinoma of the prostate other than biopsy or turp, including patients previously on hormone therapy for treatment of their prostate cancer
    boolean
    C0087111 (UMLS CUI [1])
    C0600139 (UMLS CUI [2])
    malignancies
    Item
    prior or active malignancy other than non-melanoma skin cancer; or colon or thyroid cancer treated a minimum of five years prior to study entry and presumed cured
    boolean
    C0006826 (UMLS CUI [1])
    tumor volume
    Item
    simulated volume exceeds 1000 cm3
    boolean
    C0475276 (UMLS CUI [1])
    previous pelvic radiotherapy
    Item
    previous pelvic radiotherapy
    boolean
    C1522449 (UMLS CUI [1,1])
    C0030797 (UMLS CUI [1,2])
    inflammatory bowel disease
    Item
    inflammatory bowel disease
    boolean
    C0021390 (UMLS CUI [1])
    comorbidity precluding radiotherapy or surgical biopsy
    Item
    serious non-malignant disease which would preclude radiotherapy or surgical biopsy
    boolean
    C1321605 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    geographic inaccessibility for follow-up
    Item
    geographic inaccessibility for follow-up
    boolean
    C1321605 (UMLS CUI [1])
    psychiatric or addictive disorder precluding consent or compliance
    Item
    psychiatric or addictive disorder which would preclude obtaining informed consent or adherence to protocol
    boolean
    C1321605 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    unable to commence radiation therapy within 26 weeks
    Item
    unable to commence radiation therapy within 26 weeks of the date of last prostatic biopsy
    boolean
    C1321605 (UMLS CUI [1])
    failure to give informed consent
    Item
    failure to give informed consent to participate in the study
    boolean
    C0021430 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])

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