0 Evaluaciones
ID

37770

Descripción

Study ID: 104864/627 Clinical Study ID: 104864/627 Study Title: An Open-label, Multicenter, Non-Comparative Phase II Study of the Combination of Intravenous Topotecan and Gemcitabine Administered Once Weekly for Three Weeks Every 28 Days as Second-line Treatment in Patients With Recurrent Platinum Sensitive Ovarian Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00061308 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan, Gemcitabine Study Indication: Peritoneal Cancer, Ovarian Cancer, Neoplasms, Ovarian, Fallopian Tube Cancer

Palabras clave

Versiones (2)
  1. 22.08.19 22.08.19 -
  2. 23.08.19 23.08.19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

23. August 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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    Intravenous Topotecan and Gemcitabine as Second-line Treatment in Patients With Ovarian Cancer NCT00061308

    Inglés

    Screening - Significant Medical/ Surgical History and Physical Examination; History of Ovarian Cancer; Tumor Marker

    1 formularios  
    Administrative
    Descripción

    Administrative

    Alias
    UMLS CUI-1
    C1320722
    Center Number
    Descripción

    Center Number

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C1301943
    UMLS CUI [1,2]
    C0600091
    Patient Number
    Descripción

    Patient Number

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C1709561
    Patient ID
    Descripción

    Patient ID

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2348585
    Significant Medical/ Surgical History and Physical Examination
    Descripción

    Significant Medical/ Surgical History and Physical Examination

    Alias
    UMLS CUI-1
    C0262926
    UMLS CUI-2
    C0489540
    UMLS CUI-3
    C0031809
    Is the patient suffering from or has she ever suffered from any significant medical or surgical condition not related to the study indication?
    Descripción

    If ”Yes“, please provide diagnosis below listing no more than one diagnosis per line.

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0543467
    UMLS CUI [2]
    C0012634
    UMLS CUI [3,1]
    C2603343
    UMLS CUI [3,2]
    C3146298
    UMLS CUI [3,3]
    C0439849
    Significant Medical/ Surgical History and Physical Examination
    Descripción

    Significant Medical/ Surgical History and Physical Examination

    Alias
    UMLS CUI-1
    C0262926
    UMLS CUI-2
    C0489540
    UMLS CUI-3
    C0031809
    Diagnosis
    Descripción

    Diagnosis

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0011900
    Date of Diagnosis
    Descripción

    Date of Diagnosis

    Tipo de datos

    partialDate

    Alias
    UMLS CUI [1]
    C2316983
    Status of Disease
    Descripción

    Status of Disease

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C0699749
    History of Ovarian Cancer
    Descripción

    History of Ovarian Cancer

    Alias
    UMLS CUI-1
    C0029925
    UMLS CUI-2
    C0262926
    Date of Original Diagnosis
    Descripción

    Date of Original Diagnosis

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C2316983
    Date of Relapse
    Descripción

    Date of Relapse

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0035020
    UMLS CUI [1,2]
    C0011008
    Primary Tumor Diagnosis
    Descripción

    (please choose one)

    Tipo de datos

    integer

    Alias
    UMLS CUI [1,1]
    C0677930
    UMLS CUI [1,2]
    C0011900
    Please record the current TNM stage of the patient
    Descripción

    Please record the current TNM stage of the patient

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C1302362
    FIGO Stage of current disease
    Descripción

    (please choose one) NOTE: Patient is ONL Y eligible if she is stage IIIB, IIIC or IV.

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C0450454
    Metastatic
    Descripción

    Metastatic

    Alias
    UMLS CUI-1
    C0027627
    Metastasis - Date of Diagnosis
    Descripción

    Metastasis - Date of Diagnosis

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C2316983
    UMLS CUI [1,2]
    C0027627
    Metastasis - Site
    Descripción

    Metastasis - Site

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C0807944
    If other site of metastasis, specify.
    Descripción

    If other site of metastasis, specify.

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0807944
    UMLS CUI [1,2]
    C0205394
    UMLS CUI [1,3]
    C2348235
    Tumor Marker (CA-125) (7 days prior to Day 1)
    Descripción

    Tumor Marker (CA-125) (7 days prior to Day 1)

    Alias
    UMLS CUI-1
    C0474700
    UMLS CUI-2
    C0201549
    Sample Date
    Descripción

    Sample Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C1302413
    Laboratory Name
    Descripción

    Laboratory Name

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C3258037
    CA-125 Value
    Descripción

    CA-125 Value

    Tipo de datos

    integer

    Unidades de medida
    • U/mL
    Alias
    UMLS CUI [1]
    C0201549
    U/mL
    Volver a la parte superior de la página

    Similar models

    Screening - Significant Medical/ Surgical History and Physical Examination; History of Ovarian Cancer; Tumor Marker

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Administrative
    C1320722 (UMLS CUI-1)
    Center Number
    Item
    Center Number
    text
    C1301943 (UMLS CUI [1,1])
    C0600091 (UMLS CUI [1,2])
    Patient Number
    Item
    Patient Number
    text
    C1709561 (UMLS CUI [1])
    Patient ID
    Item
    Patient ID
    text
    C2348585 (UMLS CUI [1])
    Item Group
    Significant Medical/ Surgical History and Physical Examination
    C0262926 (UMLS CUI-1)
    C0489540 (UMLS CUI-2)
    C0031809 (UMLS CUI-3)
    Is the patient suffering from or has she ever suffered from any significant medical or surgical condition not related to the study indication?
    Item
    Is the patient suffering from or has she ever suffered from any significant medical or surgical condition not related to the study indication?
    boolean
    C0543467 (UMLS CUI [1])
    C0012634 (UMLS CUI [2])
    C2603343 (UMLS CUI [3,1])
    C3146298 (UMLS CUI [3,2])
    C0439849 (UMLS CUI [3,3])
    Item Group
    Significant Medical/ Surgical History and Physical Examination
    C0262926 (UMLS CUI-1)
    C0489540 (UMLS CUI-2)
    C0031809 (UMLS CUI-3)
    Diagnosis
    Item
    Diagnosis
    text
    C0011900 (UMLS CUI [1])
    Date of Diagnosis
    Item
    Date of Diagnosis
    partialDate
    C2316983 (UMLS CUI [1])
    Item
    Status of Disease
    integer
    C0699749 (UMLS CUI [1])
    Status of Disease
    Code List
    Status of Disease
    CL Item
    Past (1)
    CL Item
    Current/ Active (2)
    Item Group
    History of Ovarian Cancer
    C0029925 (UMLS CUI-1)
    C0262926 (UMLS CUI-2)
    Date of Original Diagnosis
    Item
    Date of Original Diagnosis
    date
    C2316983 (UMLS CUI [1])
    Date of Relapse
    Item
    Date of Relapse
    date
    C0035020 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Primary Tumor Diagnosis
    integer
    C0677930 (UMLS CUI [1,1])
    C0011900 (UMLS CUI [1,2])
    Primary Tumor Diagnosis
    Code List
    Primary Tumor Diagnosis
    CL Item
    Epithelial ovarian carcinoma  (1)
    CL Item
    Primary peritoneal carcinoma  (2)
    CL Item
    Fallopian tube carcinoma  (3)
    CL Item
    Tumors of mixed mullerian origin (4)
    Please record the current TNM stage of the patient
    Item
    Please record the current TNM stage of the patient
    text
    C1302362 (UMLS CUI [1])
    Item
    FIGO Stage of current disease
    integer
    C0450454 (UMLS CUI [1])
    FIGO Stage of current disease
    Code List
    FIGO Stage of current disease
    CL Item
    IIIB Macroscopic peritoneal metastasis beyond pelvis 2 cm or less in greatest dimension.  (1)
    CL Item
    IIIC Peritoneal metastasis beyond pelvis more than 2 cm in greatest dimension and/or regional lymph node metastasis.  (2)
    CL Item
    IV Distant metastasis (excludes peritoneal metastasis). (3)
    Item Group
    Metastatic
    C0027627 (UMLS CUI-1)
    Metastasis - Date of Diagnosis
    Item
    Metastasis - Date of Diagnosis
    date
    C2316983 (UMLS CUI [1,1])
    C0027627 (UMLS CUI [1,2])
    Item
    Metastasis - Site
    integer
    C0807944 (UMLS CUI [1])
    Metastasis - Site
    Code List
    Metastasis - Site
    CL Item
    Lymph Node  (1)
    CL Item
    Liver  (2)
    CL Item
    Other, Specify. (3)
    If other site of metastasis, specify.
    Item
    If other site of metastasis, specify.
    text
    C0807944 (UMLS CUI [1,1])
    C0205394 (UMLS CUI [1,2])
    C2348235 (UMLS CUI [1,3])
    Item Group
    Tumor Marker (CA-125) (7 days prior to Day 1)
    C0474700 (UMLS CUI-1)
    C0201549 (UMLS CUI-2)
    Sample Date
    Item
    Sample Date
    date
    C1302413 (UMLS CUI [1])
    Laboratory Name
    Item
    Laboratory Name
    text
    C3258037 (UMLS CUI [1])
    CA-125 Value
    Item
    CA-125 Value
    integer
    C0201549 (UMLS CUI [1])
    Volver a la parte superior de la página 

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