0 Ratings

ID

44719

Description

see http://clinicaltrials.gov/ct2/show/record/NCT00617669 Phase III Trial of ZD4054 (Zibotentan) (Endothelin A Antagonist) and Docetaxel in Metastatic Hormone Resistant Prostate Cancer

Link

http://clinicaltrials.gov/ct2/show/record/NCT00617669

Keywords

  1. 11/15/11 11/15/11 -
  2. 3/23/14 3/23/14 - Martin Dugas
  3. 8/10/14 8/10/14 - Martin Dugas
  4. 4/13/21 4/13/21 - Dr. rer. medic Philipp Neuhaus
  5. 9/20/21 9/20/21 -
  6. 9/28/21 9/28/21 - Sarah Riepenhausen
Copyright Holder

AstraZeneca

Uploaded on

September 28, 2021

DOI

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License

Creative Commons BY 4.0

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    Eligibility DRKS00005404 NCT00617669 Prostate Cancer

    Eligibility NCT00617669

    1. StudyEvent: Eligibility
      1. Eligibility NCT00617669
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI-1
    C1512693
    18 Years and older
    Description

    Age

    Data type

    integer

    Measurement units
    • years
    Alias
    UMLS CUI-1
    C0001779
    years
    male
    Description

    Gender Male

    Data type

    boolean

    Alias
    UMLS CUI-1
    C0086582
    Confirmed diagnosis of prostate cancer (adenocarcinoma of the prostate) that has spread to the bone (bone metastasis)
    Description

    Prostate Cancer with bone metastasis

    Data type

    boolean

    Alias
    UMLS CUI-1
    C0600139
    UMLS CUI-2
    C0153690
    Increasing Prostate Specific Antigen (PSA), collected within one year of enrollment
    Description

    PSA increase

    Data type

    boolean

    Alias
    UMLS CUI-1
    C0138741
    Currently receiving treatment with surgical or medical castration
    Description

    Castration

    Data type

    boolean

    Alias
    UMLS CUI-1
    C0007347
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI-1
    C0680251
    Previous treatment with chemotherapy (paclitaxel, docetaxel, and mitoxantrone). Prior targeted cancer therapies are permitted if received during a previous clinical trial
    Description

    Previous chemotherapy

    Data type

    boolean

    Alias
    UMLS CUI-1
    C0205156
    UMLS CUI-2
    C0392920
    Suffering from heart failure or had a myocardial infarction within last 6 months
    Description

    Heart disease

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0018801
    UMLS CUI [1,2]
    C0155626
    A history of epilepsy or seizures
    Description

    Epilepsy, seizures

    Data type

    boolean

    Alias
    UMLS CUI-1
    C0014544
    UMLS CUI-2
    C0036572

    Similar models

    Eligibility NCT00617669

    1. StudyEvent: Eligibility
      1. Eligibility NCT00617669
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Inclusion Criteria
    C1512693 (UMLS CUI-1)
    Age
    Item
    18 Years and older
    integer
    C0001779 (UMLS CUI-1)
    Gender Male
    Item
    male
    boolean
    C0086582 (UMLS CUI-1)
    Prostate Cancer with bone metastasis
    Item
    Confirmed diagnosis of prostate cancer (adenocarcinoma of the prostate) that has spread to the bone (bone metastasis)
    boolean
    C0600139 (UMLS CUI-1)
    C0153690 (UMLS CUI-2)
    PSA increase
    Item
    Increasing Prostate Specific Antigen (PSA), collected within one year of enrollment
    boolean
    C0138741 (UMLS CUI-1)
    Castration
    Item
    Currently receiving treatment with surgical or medical castration
    boolean
    C0007347 (UMLS CUI-1)
    Item Group
    Exclusion Criteria
    C0680251 (UMLS CUI-1)
    Previous chemotherapy
    Item
    Previous treatment with chemotherapy (paclitaxel, docetaxel, and mitoxantrone). Prior targeted cancer therapies are permitted if received during a previous clinical trial
    boolean
    C0205156 (UMLS CUI-1)
    C0392920 (UMLS CUI-2)
    Heart disease
    Item
    Suffering from heart failure or had a myocardial infarction within last 6 months
    boolean
    C0018801 (UMLS CUI [1,1])
    C0155626 (UMLS CUI [1,2])
    Epilepsy, seizures
    Item
    A history of epilepsy or seizures
    boolean
    C0014544 (UMLS CUI-1)
    C0036572 (UMLS CUI-2)

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