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ID

13518

Description

Pilot Clinical Trial of Pazopanib in Patients With Relapsed or Refractory Acute Myeloid Leukemia (AML) or at Initial Diagnosis When no Intensive Treatment is Possible (PAZOPANIB-AML) https://clinicaltrials.gov/ct2/show/NCT01361334 Principal Investigator: PD Dr. Torsten Kessler, University Hospital Muenster, Germany

Link

https://clinicaltrials.gov/ct2/show/NCT01361334

Keywords

  1. 8/14/15 8/14/15 - Martin Dugas
  2. 1/11/16 1/11/16 -
  3. 2/11/16 2/11/16 -
Uploaded on

February 11, 2016

DOI

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License

Creative Commons BY 4.0

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    Clinical examination AML Pazopanib NCT01361334

    Clinical examination AML Pazopanib NCT01361334

    Clinical Examination
    Description

    Clinical Examination

    Alias
    UMLS CUI-1
    C0582103
    Patient ID (derived)
    Description

    Patient ID (derived)

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Visit info/Therapeutic regimen timepoint
    Description

    Visit info

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1276413
    UMLS CUI [1,2]
    C2348792
    Visit done: yes
    Description

    Durchführung der Visite: Ja

    Data type

    text

    Alias
    UMLS CUI [1]
    C0008952
    Date of visit, from visit 2 on
    Description

    Visitendatum ab Visite 2

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0008952
    UMLS CUI [1,2]
    C0011008
    Date of visit, from visit 2 on - status
    Description

    Visitendatum ab Visite 2 Status

    Data type

    text

    Alias
    UMLS CUI [1]
    C0008952
    Visit done: no, but Patient stays on study
    Description

    Durchführung der Visite: Nein

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0008952
    UMLS CUI [1,2]
    C2348568
    Visit done: patient off study
    Description

    Durchführung der Visite: Studienabbruch

    Data type

    text

    Alias
    UMLS CUI [1]
    C1518546
    Clinical findings: date
    Description

    Klinischer Befund: Datum

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0582103
    UMLS CUI [1,2]
    C0011008
    Clinical findings, status date
    Description

    Klinischer Befund: Datum Status

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0582103
    UMLS CUI [1,2]
    C2985875
    ECOG-status
    Description

    ECOG

    Data type

    text

    Alias
    UMLS CUI [1]
    C1520224
    ECOG-status: nd
    Description

    ECOG-Status: nd

    Data type

    text

    Alias
    UMLS CUI [1]
    C1520224
    Weight
    Description

    Weight

    Data type

    integer

    Measurement units
    • kg
    Alias
    UMLS CUI [1]
    C0005910
    kg
    Weight: nd
    Description

    Gewicht: nd

    Data type

    text

    Alias
    UMLS CUI [1]
    C0005910
    Height
    Description

    Height

    Data type

    integer

    Measurement units
    • cm
    Alias
    UMLS CUI [1]
    C0005890
    cm
    Pulse/Heart rate
    Description

    Pulse

    Data type

    integer

    Measurement units
    • /min
    Alias
    UMLS CUI [1]
    C0018810
    /min
    Pulse/HR: not done
    Description

    Puls: nd

    Data type

    text

    Alias
    UMLS CUI [1]
    C0018810
    Systolic blood pressure
    Description

    systolic

    Data type

    integer

    Measurement units
    • mmHg
    Alias
    UMLS CUI [1]
    C0871470
    mmHg
    Diastolic blood pressure
    Description

    diastolic

    Data type

    integer

    Measurement units
    • mmHg
    Alias
    UMLS CUI [1]
    C0428883
    mmHg
    Blood pressure: not done
    Description

    Blutdruck: nd

    Data type

    text

    Alias
    UMLS CUI [1]
    C0005823
    QT interval
    Description

    QT interval

    Data type

    integer

    Measurement units
    • ms
    Alias
    UMLS CUI [1]
    C1287082
    ms
    ECG (QT-time): nd
    Description

    EKG (QT-Zeit): nd

    Data type

    text

    Alias
    UMLS CUI [1]
    C1287082
    Clinical examination
    Description

    Clinical examination

    Data type

    text

    Alias
    UMLS CUI [1]
    C1456356
    Findings
    Description

    Findings

    Alias
    UMLS CUI-1
    C0243095
    Finding
    Description

    Finding

    Data type

    text

    Alias
    UMLS CUI [1]
    C0243095

    Similar models

    Clinical examination AML Pazopanib NCT01361334

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Clinical Examination
    C0582103 (UMLS CUI-1)
    Patient ID (derived)
    Item
    Patient ID (derived)
    text
    C2348585 (UMLS CUI [1])
    Item
    Visit info/Therapeutic regimen timepoint
    text
    C1276413 (UMLS CUI [1,1])
    C2348792 (UMLS CUI [1,2])
    Code List
    Visit info/Therapeutic regimen timepoint
    CL Item
    Baseline (1)
    CL Item
    Tag 1 (2)
    CL Item
    Tag 2 (3)
    CL Item
    Tag 7 (4)
    CL Item
    Tag 10 (5)
    CL Item
    Tag 14 (6)
    CL Item
    Tag 28 (7)
    CL Item
    Monat 2 (8)
    CL Item
    Monat 3 (9)
    CL Item
    Monat 6 (10)
    CL Item
    Monat 9 (11)
    CL Item
    Monat 12 (12)
    CL Item
    Progression - Rezidiv (13)
    CL Item
    Follow Up - Blatt Nr. 1 (14)
    CL Item
    Follow Up - Blatt Nr. 2 (15)
    CL Item
    Follow Up - Blatt Nr. 3 (16)
    CL Item
    Follow Up - Blatt Nr. 4 (17)
    Item
    Visit done: yes
    text
    C0008952 (UMLS CUI [1])
    Code List
    Visit done: yes
    CL Item
    ja (1)
    Visitendatum ab Visite 2
    Item
    Date of visit, from visit 2 on
    date
    C0008952 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Date of visit, from visit 2 on - status
    text
    C0008952 (UMLS CUI [1])
    Code List
    Date of visit, from visit 2 on - status
    CL Item
    T (1)
    CL Item
    TM (2)
    CL Item
    M (3)
    Item
    Visit done: no, but Patient stays on study
    text
    C0008952 (UMLS CUI [1,1])
    C2348568 (UMLS CUI [1,2])
    Code List
    Visit done: no, but Patient stays on study
    CL Item
    nein, Patient verbleibt aber in der Studie (0)
    Item
    Visit done: patient off study
    text
    C1518546 (UMLS CUI [1])
    Code List
    Visit done: patient off study
    CL Item
    study exit (9)
    Klinischer Befund: Datum
    Item
    Clinical findings: date
    date
    C0582103 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Clinical findings, status date
    text
    C0582103 (UMLS CUI [1,1])
    C2985875 (UMLS CUI [1,2])
    Code List
    Clinical findings, status date
    CL Item
    T (1)
    CL Item
    TM (2)
    CL Item
    M (3)
    Item
    ECOG-status
    text
    C1520224 (UMLS CUI [1])
    Code List
    ECOG-status
    CL Item
    ECOG-Status 0 (0)
    C1828078 (UMLS CUI-1)
    CL Item
    ECOG-Status 1 (1)
    C1827388 (UMLS CUI-1)
    CL Item
    ECOG-Status 2 (2)
    C1828242 (UMLS CUI-1)
    CL Item
    ECOG-Status 3 (3)
    C1827126 (UMLS CUI-1)
    CL Item
    ECOG-Status 4 (4)
    C1827528 (UMLS CUI-1)
    Item
    ECOG-status: nd
    text
    C1520224 (UMLS CUI [1])
    Code List
    ECOG-status: nd
    CL Item
    nd (9)
    Weight
    Item
    Weight
    integer
    C0005910 (UMLS CUI [1])
    Item
    Weight: nd
    text
    C0005910 (UMLS CUI [1])
    Code List
    Weight: nd
    CL Item
    nd (9)
    Height
    Item
    Height
    integer
    C0005890 (UMLS CUI [1])
    Pulse
    Item
    Pulse/Heart rate
    integer
    C0018810 (UMLS CUI [1])
    Item
    Pulse/HR: not done
    text
    C0018810 (UMLS CUI [1])
    Code List
    Pulse/HR: not done
    CL Item
    nd (9)
    systolic
    Item
    Systolic blood pressure
    integer
    C0871470 (UMLS CUI [1])
    diastolic
    Item
    Diastolic blood pressure
    integer
    C0428883 (UMLS CUI [1])
    Item
    Blood pressure: not done
    text
    C0005823 (UMLS CUI [1])
    Code List
    Blood pressure: not done
    CL Item
    nd (9)
    QT interval
    Item
    QT interval
    integer
    C1287082 (UMLS CUI [1])
    Item
    ECG (QT-time): nd
    text
    C1287082 (UMLS CUI [1])
    Code List
    ECG (QT-time): nd
    CL Item
    nd (9)
    Item
    Clinical examination
    text
    C1456356 (UMLS CUI [1])
    Code List
    Clinical examination
    CL Item
    without pathological findings  (1)
    CL Item
    pathologic findings, please specify (2)
    Item Group
    Findings
    C0243095 (UMLS CUI-1)
    Finding
    Item
    Finding
    text
    C0243095 (UMLS CUI [1])

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