ID

18132

Descripción

MRI Study of BAY 43-9006 in Metastatic Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00606866

Link

https://clinicaltrials.gov/show/NCT00606866

Palabras clave

  1. 21.10.16 21.10.16 -
Subido en

21. Oktober 2016

DOI

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Licencia

Creative Commons BY 4.0

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    Eligibility Metastatic Renal Cell Carcinoma NCT00606866

    Eligibility Metastatic Renal Cell Carcinoma NCT00606866

    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    histologically or cytologically confirmed metastatic clear cell renal cell cancer;
    Descripción

    Clear Cell Renal Cell Carcinoma Metastatic

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0279702
    UMLS CUI [1,2]
    C0036525
    at least one lesion that can be accurately measured in at least one dimension;
    Descripción

    Measurable Disease Linear Quantity

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1513041
    UMLS CUI [1,2]
    C0205132
    UMLS CUI [1,3]
    C1265611
    patients must not have been treated with prior anti-timor kinase inhibitors or vegf pathway inhibitors;
    Descripción

    Kinase Inhibitors Against Malignant Neoplasms | VEGF Signaling Pathway inhibitors

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1152564
    UMLS CUI [1,2]
    C0521124
    UMLS CUI [1,3]
    C0006826
    UMLS CUI [2,1]
    C2984329
    UMLS CUI [2,2]
    C0243077
    age 18 and older;
    Descripción

    Age

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    ecog performance status 0-2;
    Descripción

    ECOG performance status

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    blood pressure higher than 140/90 on 2 separate occasions not more than 6 weeks prior to enrollment and not less than 24 hours apart;
    Descripción

    Blood pressure finding Quantity

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1271104
    UMLS CUI [1,2]
    C1265611
    normal organ function: total bilirubin less than upper limit of normal, ast less than 2.5 x upper limit of normal, creatinine less than 2.8 mg/dl;
    Descripción

    organ function | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Creatinine measurement, serum

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0678852
    UMLS CUI [2]
    C1278039
    UMLS CUI [3]
    C0201899
    UMLS CUI [4]
    C0201976
    women of child-bearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation;
    Descripción

    Childbearing Potential Contraceptive methods | Gender Contraceptive methods

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3831118
    UMLS CUI [1,2]
    C0700589
    UMLS CUI [2,1]
    C0079399
    UMLS CUI [2,2]
    C0700589
    ability to understand and the willingness to sign a written informed consent document.
    Descripción

    Informed Consent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    chemotherapy or radiotherapy within 4 weeks prior to entering the study;
    Descripción

    Chemotherapy | Therapeutic radiology procedure

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    UMLS CUI [2]
    C1522449
    any other investigational agents;
    Descripción

    Investigational New Drugs

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0013230
    known brain metastases;
    Descripción

    Metastatic malignant neoplasm to brain

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0220650
    uncontrolled intercurrent illness including ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements;
    Descripción

    Illness Uncontrolled | Communicable Diseases | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Mental disorders Compliance behavior Limited | social situation Compliance behavior Limited

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0221423
    UMLS CUI [1,2]
    C0205318
    UMLS CUI [2]
    C0009450
    UMLS CUI [3]
    C0742758
    UMLS CUI [4]
    C0002965
    UMLS CUI [5]
    C0003811
    UMLS CUI [6,1]
    C0004936
    UMLS CUI [6,2]
    C1321605
    UMLS CUI [6,3]
    C0439801
    UMLS CUI [7,1]
    C0748872
    UMLS CUI [7,2]
    C1321605
    UMLS CUI [7,3]
    C0439801
    pregnancy.
    Descripción

    Pregnancy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032961

    Similar models

    Eligibility Metastatic Renal Cell Carcinoma NCT00606866

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Clear Cell Renal Cell Carcinoma Metastatic
    Item
    histologically or cytologically confirmed metastatic clear cell renal cell cancer;
    boolean
    C0279702 (UMLS CUI [1,1])
    C0036525 (UMLS CUI [1,2])
    Measurable Disease Linear Quantity
    Item
    at least one lesion that can be accurately measured in at least one dimension;
    boolean
    C1513041 (UMLS CUI [1,1])
    C0205132 (UMLS CUI [1,2])
    C1265611 (UMLS CUI [1,3])
    Kinase Inhibitors Against Malignant Neoplasms | VEGF Signaling Pathway inhibitors
    Item
    patients must not have been treated with prior anti-timor kinase inhibitors or vegf pathway inhibitors;
    boolean
    C1152564 (UMLS CUI [1,1])
    C0521124 (UMLS CUI [1,2])
    C0006826 (UMLS CUI [1,3])
    C2984329 (UMLS CUI [2,1])
    C0243077 (UMLS CUI [2,2])
    Age
    Item
    age 18 and older;
    boolean
    C0001779 (UMLS CUI [1])
    ECOG performance status
    Item
    ecog performance status 0-2;
    boolean
    C1520224 (UMLS CUI [1])
    Blood pressure finding Quantity
    Item
    blood pressure higher than 140/90 on 2 separate occasions not more than 6 weeks prior to enrollment and not less than 24 hours apart;
    boolean
    C1271104 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    organ function | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Creatinine measurement, serum
    Item
    normal organ function: total bilirubin less than upper limit of normal, ast less than 2.5 x upper limit of normal, creatinine less than 2.8 mg/dl;
    boolean
    C0678852 (UMLS CUI [1])
    C1278039 (UMLS CUI [2])
    C0201899 (UMLS CUI [3])
    C0201976 (UMLS CUI [4])
    Childbearing Potential Contraceptive methods | Gender Contraceptive methods
    Item
    women of child-bearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation;
    boolean
    C3831118 (UMLS CUI [1,1])
    C0700589 (UMLS CUI [1,2])
    C0079399 (UMLS CUI [2,1])
    C0700589 (UMLS CUI [2,2])
    Informed Consent
    Item
    ability to understand and the willingness to sign a written informed consent document.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Chemotherapy | Therapeutic radiology procedure
    Item
    chemotherapy or radiotherapy within 4 weeks prior to entering the study;
    boolean
    C0392920 (UMLS CUI [1])
    C1522449 (UMLS CUI [2])
    Investigational New Drugs
    Item
    any other investigational agents;
    boolean
    C0013230 (UMLS CUI [1])
    Metastatic malignant neoplasm to brain
    Item
    known brain metastases;
    boolean
    C0220650 (UMLS CUI [1])
    Illness Uncontrolled | Communicable Diseases | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Mental disorders Compliance behavior Limited | social situation Compliance behavior Limited
    Item
    uncontrolled intercurrent illness including ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements;
    boolean
    C0221423 (UMLS CUI [1,1])
    C0205318 (UMLS CUI [1,2])
    C0009450 (UMLS CUI [2])
    C0742758 (UMLS CUI [3])
    C0002965 (UMLS CUI [4])
    C0003811 (UMLS CUI [5])
    C0004936 (UMLS CUI [6,1])
    C1321605 (UMLS CUI [6,2])
    C0439801 (UMLS CUI [6,3])
    C0748872 (UMLS CUI [7,1])
    C1321605 (UMLS CUI [7,2])
    C0439801 (UMLS CUI [7,3])
    Pregnancy
    Item
    pregnancy.
    boolean
    C0032961 (UMLS CUI [1])

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