0 Ratings
ID

17554

Description

Gemcitabine, Oxaliplatin in Combination With Bevacizumab in Patients With Hepatocellular Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00142467

Link

https://clinicaltrials.gov/show/NCT00142467

Keywords

Versions (1)
  1. 9/23/16 9/23/16 -
Uploaded on

September 23, 2016

DOI

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License

Creative Commons BY 4.0
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    Eligibility Hepatocellular Carcinoma NCT00142467

    English

    Eligibility Hepatocellular Carcinoma NCT00142467

    1 forms  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    unresectable or metastatic hepatocellular carcinoma
    Description

    Liver cell carcinoma non-resectable | Metastatic hepatocellular carcinoma

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1112459
    UMLS CUI [2]
    C0744869
    measurable tumors
    Description

    Measurable Disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1513041
    adequate hepatic function: total bilirubin < 3.0mg/dl; ast < 7x uln
    Description

    Liver function | Serum total bilirubin measurement | Aspartate aminotransferase measurement

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0232741
    UMLS CUI [2]
    C1278039
    UMLS CUI [3]
    C0201899
    adequate bone marrow function: anc > 1,000/mm3; platelets > 75,000/mm3
    Description

    Bone Marrow function | Absolute neutrophil count | Platelet Count measurement

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0005953
    UMLS CUI [1,2]
    C0031843
    UMLS CUI [2]
    C0948762
    UMLS CUI [3]
    C0032181
    inr < 1.5 for those who are not on anticoagulation
    Description

    INR | Anticoagulation Therapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0525032
    UMLS CUI [2]
    C0003281
    up to two prior chemotherapy regimens for hepatocellular carcinoma
    Description

    Prior Chemotherapy Quantity Liver carcinoma

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1514457
    UMLS CUI [1,2]
    C1265611
    UMLS CUI [1,3]
    C2239176
    18 years of age or older
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    ecog performance status of 0-1
    Description

    ECOG performance status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    life expectancy of > 12 weeks
    Description

    Life Expectancy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023671
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    clinically apparent central nervous system metastases or carcinomatous meningitis
    Description

    CNS metastases apparent Clinical | Meningeal Carcinomatosis

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0686377
    UMLS CUI [1,2]
    C0750489
    UMLS CUI [1,3]
    C0205210
    UMLS CUI [2]
    C0220654
    uncontrolled serious medical or psychiatric illness
    Description

    Illness Serious Uncontrolled | Mental disorders

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0221423
    UMLS CUI [1,2]
    C0205404
    UMLS CUI [1,3]
    C0205318
    UMLS CUI [2]
    C0004936
    pregnant or lactating women
    Description

    Pregnancy | Breast Feeding

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    current or recent (within 4 weeks of first study infusion) participation in experimental study drug
    Description

    Study Subject Participation Status | Investigational New Drugs

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    UMLS CUI [2]
    C0013230
    uncontrolled hypertension
    Description

    Uncontrolled hypertension

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1868885
    significant proteinuria
    Description

    Proteinuria Significant

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0033687
    UMLS CUI [1,2]
    C0750502
    serious, non-healing wound, ulcer, or bone fracture
    Description

    Non-healed wound Serious | Ulcer | Fracture

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0750433
    UMLS CUI [1,2]
    C0205404
    UMLS CUI [2]
    C0041582
    UMLS CUI [3]
    C0016658
    evidence of bleeding diathesis or coagulopathy
    Description

    Bleeding tendency Evidence of | Blood Coagulation Disorders Evidence of

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1458140
    UMLS CUI [1,2]
    C0332120
    UMLS CUI [2,1]
    C0005779
    UMLS CUI [2,2]
    C0332120
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    Similar models

    Eligibility Hepatocellular Carcinoma NCT00142467

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Liver cell carcinoma non-resectable | Metastatic hepatocellular carcinoma
    Item
    unresectable or metastatic hepatocellular carcinoma
    boolean
    C1112459 (UMLS CUI [1])
    C0744869 (UMLS CUI [2])
    Measurable Disease
    Item
    measurable tumors
    boolean
    C1513041 (UMLS CUI [1])
    Liver function | Serum total bilirubin measurement | Aspartate aminotransferase measurement
    Item
    adequate hepatic function: total bilirubin < 3.0mg/dl; ast < 7x uln
    boolean
    C0232741 (UMLS CUI [1])
    C1278039 (UMLS CUI [2])
    C0201899 (UMLS CUI [3])
    Bone Marrow function | Absolute neutrophil count | Platelet Count measurement
    Item
    adequate bone marrow function: anc > 1,000/mm3; platelets > 75,000/mm3
    boolean
    C0005953 (UMLS CUI [1,1])
    C0031843 (UMLS CUI [1,2])
    C0948762 (UMLS CUI [2])
    C0032181 (UMLS CUI [3])
    INR | Anticoagulation Therapy
    Item
    inr < 1.5 for those who are not on anticoagulation
    boolean
    C0525032 (UMLS CUI [1])
    C0003281 (UMLS CUI [2])
    Prior Chemotherapy Quantity Liver carcinoma
    Item
    up to two prior chemotherapy regimens for hepatocellular carcinoma
    boolean
    C1514457 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    C2239176 (UMLS CUI [1,3])
    Age
    Item
    18 years of age or older
    boolean
    C0001779 (UMLS CUI [1])
    ECOG performance status
    Item
    ecog performance status of 0-1
    boolean
    C1520224 (UMLS CUI [1])
    Life Expectancy
    Item
    life expectancy of > 12 weeks
    boolean
    C0023671 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    CNS metastases apparent Clinical | Meningeal Carcinomatosis
    Item
    clinically apparent central nervous system metastases or carcinomatous meningitis
    boolean
    C0686377 (UMLS CUI [1,1])
    C0750489 (UMLS CUI [1,2])
    C0205210 (UMLS CUI [1,3])
    C0220654 (UMLS CUI [2])
    Illness Serious Uncontrolled | Mental disorders
    Item
    uncontrolled serious medical or psychiatric illness
    boolean
    C0221423 (UMLS CUI [1,1])
    C0205404 (UMLS CUI [1,2])
    C0205318 (UMLS CUI [1,3])
    C0004936 (UMLS CUI [2])
    Pregnancy | Breast Feeding
    Item
    pregnant or lactating women
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Study Subject Participation Status | Investigational New Drugs
    Item
    current or recent (within 4 weeks of first study infusion) participation in experimental study drug
    boolean
    C2348568 (UMLS CUI [1])
    C0013230 (UMLS CUI [2])
    Uncontrolled hypertension
    Item
    uncontrolled hypertension
    boolean
    C1868885 (UMLS CUI [1])
    Proteinuria Significant
    Item
    significant proteinuria
    boolean
    C0033687 (UMLS CUI [1,1])
    C0750502 (UMLS CUI [1,2])
    Non-healed wound Serious | Ulcer | Fracture
    Item
    serious, non-healing wound, ulcer, or bone fracture
    boolean
    C0750433 (UMLS CUI [1,1])
    C0205404 (UMLS CUI [1,2])
    C0041582 (UMLS CUI [2])
    C0016658 (UMLS CUI [3])
    Bleeding tendency Evidence of | Blood Coagulation Disorders Evidence of
    Item
    evidence of bleeding diathesis or coagulopathy
    boolean
    C1458140 (UMLS CUI [1,1])
    C0332120 (UMLS CUI [1,2])
    C0005779 (UMLS CUI [2,1])
    C0332120 (UMLS CUI [2,2])
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