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ID

16545

Description

Study Sponsor: Astellas Study Title Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study Medicine or Vaccine (generic name) capsaicin Sponsor Identification Number QTZ-EC-0002 Trial Registry Identification Number(#'s) NCT01416116 EudraCT Number: 2010-023258-34 Medical Condition Neuropathic pain Phase Phase 4 http://clinicaltrials.gov/show/NCT01416116 Screening Visit Form 3/4: Laboratory Tests: Hematology Laboratory Tests: Biochemistry

Link

http://clinicaltrials.gov/show/NCT01416116

Keywords

  1. 7/23/16 7/23/16 -
  2. 7/23/16 7/23/16 -
Uploaded on

July 23, 2016

DOI

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License

Creative Commons BY 4.0

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    Screening Visit Form 3/4: Laboratory tests Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116

    Screening Visit Form 3/4: Laboratory tests Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116

    Laboratory Tests: Hematology
    Description

    Laboratory Tests: Hematology

    Were samples taken?
    Description

    blood samples taken

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1277698
    Date of Sample Taken
    Description

    Date of blood Sample Taken

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C1277698
    UMLS CUI [1,2]
    C0011008
    LAB Interpretation
    Description

    LAB Interpretation

    Data type

    integer

    Alias
    UMLS CUI [1]
    C3244125
    Laboratory Tests: Hematology, specification
    Description

    Laboratory Tests: Hematology, specification

    Lab Test
    Description

    Lab Test

    Data type

    text

    Alias
    UMLS CUI [1]
    C0587081
    LAB Interpretation
    Description

    LAB Interpretation

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0587081
    UMLS CUI [1,2]
    C2826293
    Laboratory Tests: Biochemistry
    Description

    Laboratory Tests: Biochemistry

    Were samples taken?
    Description

    blood samples taken

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1277698
    Date of Sample Taken
    Description

    Date of Sample Taken

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C1277698
    UMLS CUI [1,2]
    C0011008
    LAB Interpretation
    Description

    LAB Interpretation

    Data type

    integer

    Alias
    UMLS CUI [1]
    C3244125
    Tests: Biochemistry, specification
    Description

    Tests: Biochemistry, specification

    Lab Test
    Description

    Lab Test

    Data type

    text

    Alias
    UMLS CUI [1]
    C0587081
    LAB Interpretation
    Description

    LAB Interpretation

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0587081
    UMLS CUI [1,2]
    C2826293

    Similar models

    Screening Visit Form 3/4: Laboratory tests Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Laboratory Tests: Hematology
    Item
    Were samples taken?
    integer
    C1277698 (UMLS CUI [1])
    Code List
    Were samples taken?
    CL Item
    No (0 )
    CL Item
    Yes (1 )
    Date of blood Sample Taken
    Item
    Date of Sample Taken
    date
    C1277698 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    LAB Interpretation
    integer
    C3244125 (UMLS CUI [1])
    Code List
    LAB Interpretation
    CL Item
    Normal (0 )
    CL Item
    Abnormal (1 )
    Item Group
    Laboratory Tests: Hematology, specification
    Item
    Lab Test
    text
    C0587081 (UMLS CUI [1])
    Code List
    Lab Test
    CL Item
    Red Blood Cell Count (RBC )
    CL Item
    White Blood Cell Count (WBC )
    CL Item
    Lymphocytes (LYMPH )
    CL Item
    Neutrophils (NEUT )
    CL Item
    Eosinophils (EOS )
    CL Item
    Basophils (BASO )
    CL Item
    Monocytes (MONO )
    CL Item
    Hemoglobin (HGB )
    CL Item
    Hematocrit (HCT )
    CL Item
    Platelets (PLT )
    Item
    LAB Interpretation
    text
    C0587081 (UMLS CUI [1,1])
    C2826293 (UMLS CUI [1,2])
    Code List
    LAB Interpretation
    CL Item
    Abnormal - not clinically significant (1 )
    CL Item
    Abnormal - clinically significant (2 )
    Item Group
    Laboratory Tests: Biochemistry
    Item
    Were samples taken?
    integer
    C1277698 (UMLS CUI [1])
    Code List
    Were samples taken?
    CL Item
    No (0 )
    CL Item
    Yes (1 )
    Date of Sample Taken
    Item
    Date of Sample Taken
    date
    C1277698 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    LAB Interpretation
    integer
    C3244125 (UMLS CUI [1])
    Code List
    LAB Interpretation
    CL Item
    Normal (0 )
    CL Item
    Abnormal (1 )
    Item Group
    Tests: Biochemistry, specification
    Item
    Lab Test
    text
    C0587081 (UMLS CUI [1])
    Code List
    Lab Test
    CL Item
    AST (AST )
    CL Item
    ALT (ALT )
    CL Item
    Alkaline Phosphatase (ALKP )
    CL Item
    Chloride (CL )
    CL Item
    Sodium (NA )
    CL Item
    Potassium (K )
    CL Item
    Blood urea nitrogen (BUN )
    CL Item
    Creatinine (CREAT )
    Item
    LAB Interpretation
    integer
    C0587081 (UMLS CUI [1,1])
    C2826293 (UMLS CUI [1,2])
    Code List
    LAB Interpretation
    CL Item
    Abnormal - not clinically significant (1 )
    CL Item
    Abnormal - clinically significant (2 )

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