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ID

27575

Description

Prospective Multicenter Phase III Trial Using CRS With / Without HIPEC After Preoperative Chemotherapy in Patients With Peritoneal Carcinomatosis of Gastric Cancer Incl. Adenocarcinoma of the Esophagogastric Junction NCT-Identifier: NCT02158988 Source: Prof. Dr. med. Beate Rau, MBA Charité Universitätsmedizin Berlin Weitere Follow up (ab Monat 12 bis Studienende)

Keywords

Versions (1)
  1. 11/20/17 11/20/17 -
Copyright Holder

Beate Rau

Uploaded on

November 20, 2017

DOI

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License

Creative Commons BY-NC 3.0
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    Cytoreductive Surgery (CRS) With/Without HIPEC in Gastric Cancer With Peritoneal Carcinomatosis (GASTRIPEC)

    German English

    Weitere Follow up

    1 forms  
    1. StudyEvent: ODM
      1. Weitere Follow up
    Administrative Documentation
    Description

    Administrative Documentation

    Alias
    UMLS CUI-1
    C1320722
    Center Identification
    Description

    Center Identification

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1301943
    UMLS CUI [1,2]
    C0600091
    Patient Identification
    Description

    Patient Identification

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Year of birth
    Description

    Year of birth

    Data type

    partialDate

    Alias
    UMLS CUI [1]
    C2826771
    Number of Follow up
    Description

    Number of Follow up

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C1704685
    UMLS CUI [1,2]
    C0237753
    Physical Examination
    Description

    Physical Examination

    Alias
    UMLS CUI-1
    C0031809
    Date of Examination
    Description

    Date of Examination

    Data type

    date

    Alias
    UMLS CUI [1]
    C2826643
    Weight
    Description

    Weight

    Data type

    float

    Measurement units
    • kg
    Alias
    UMLS CUI [1]
    C0005910
    kg
    Karnofsky-Index
    Description

    Karnofsky-Index

    Data type

    integer

    Measurement units
    • %
    Alias
    UMLS CUI [1]
    C0206065
    %
    Laboratory Data
    Description

    Laboratory Data

    Alias
    UMLS CUI-1
    C0022885
    Date of blood work
    Description

    Date of blood work

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0005834
    Diagnostic procedures
    Description

    Diagnostic procedures

    Alias
    UMLS CUI-1
    C0430022
    CT Abdomen
    Description

    CT Abdomen

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0412620
    Date of CT Abdomen
    Description

    Date of CT Abdomen

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0412620
    CT Thorax
    Description

    CT Thorax

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0202823
    CT Thorax
    Description

    CT Thorax

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0202823
    Echocardiography
    Description

    Echocardiography

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0013516
    Date of Echocardiography
    Description

    Date of Echocardiography

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0013516
    Results
    Description

    Results

    Alias
    UMLS CUI-1
    C0040405
    UMLS CUI-2
    C1274040
    Aszites
    Description

    Aszites

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0003962
    Metastases
    Description

    Metastases

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C3258247
    Peritoneal metastases
    Description

    Peritoneal metastases

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0346989
    Liver metastases
    Description

    Liver metastases

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0494165
    Lung metastases
    Description

    Lung metastases

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0153676
    Bone metastases
    Description

    Bone metastases

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0153690
    Other metastases
    Description

    Other metastases

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0027627
    UMLS CUI [1,2]
    C0205394
    Concomitant therapy
    Description

    Concomitant therapy

    Alias
    UMLS CUI-1
    C1707479
    Concomitant therapy
    Description

    Concomitant therapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1707479
    Tumorspecific therapy
    Description

    Tumorspecific therapy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1707479
    UMLS CUI [1,2]
    C0006826
    UMLS CUI [1,3]
    C1552740
    Complication specific therapy
    Description

    Complication specific therapy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1707479
    UMLS CUI [1,2]
    C0009566
    UMLS CUI [1,3]
    C1552740
    Supportive therapy
    Description

    Supportive therapy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0344211
    UMLS CUI [1,2]
    C1707479
    Other therapy
    Description

    Other therapy

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0418967
    UMLS CUI [1,2]
    C1707479
    Other therapy
    Description

    Other therapy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0418967
    UMLS CUI [1,2]
    C1707479
    Toxicities
    Description

    Toxicities

    Alias
    UMLS CUI-1
    C2198186
    Late toxicities
    Description

    Late toxicities

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2198186
    Late toxicites
    Description

    Late toxicites

    Alias
    UMLS CUI-1
    C2198186
    Ifd. Number
    Description

    Ifd. Number

    Data type

    integer

    Alias
    UMLS CUI [1]
    C0237753
    Toxicity
    Description

    Toxicity

    Data type

    text

    Alias
    UMLS CUI [1]
    C2198186
    Toxicity grade
    Description

    Toxicity grade

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2826262
    Progress
    Description

    Progress

    Alias
    UMLS CUI-1
    C0242656
    Tumor progress
    Description

    Tumor progress

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0242656
    UMLS CUI [1,2]
    C0006826
    Adverse Event
    Description

    Adverse Event

    Alias
    UMLS CUI-1
    C0877248
    Adverse Event
    Description

    Adverse Event

    Data type

    text

    Alias
    UMLS CUI [1]
    C0877248
    Hospitalization
    Description

    Hospitalization

    Data type

    text

    Alias
    UMLS CUI [1]
    C0019993
    Surgical intervention
    Description

    Surgical intervention

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0549433
    UMLS CUI [1,2]
    C0242656
    UMLS CUI [1,3]
    C0006826
    Life quality
    Description

    Life quality

    Questionnaire
    Description

    Questionnaire

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0034394
    UMLS CUI [1,2]
    C0205197
    UMLS CUI [1,3]
    C0034380
    Questionnaire
    Description

    Questionnaire

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0034394
    UMLS CUI [1,2]
    C0205197
    UMLS CUI [1,3]
    C0034380
    Administrative Documentation
    Description

    Administrative Documentation

    Alias
    UMLS CUI-1
    C1320722
    Date
    Description

    Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C0011008
    Name
    Description

    Name

    Data type

    text

    Alias
    UMLS CUI [1]
    C0027365
    Signature
    Description

    Signature

    Data type

    text

    Alias
    UMLS CUI [1]
    C1519316
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    Similar models

    Weitere Follow up

    1 forms
    1. StudyEvent: ODM
      1. Weitere Follow up
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1320722 (UMLS CUI-1)
    Center Identification
    Item
    text
    C1301943 (UMLS CUI [1,1])
    C0600091 (UMLS CUI [1,2])
    Patient Identification
    Item
    integer
    C2348585 (UMLS CUI [1])
    Year of birth
    Item
    partialDate
    C2826771 (UMLS CUI [1])
    Number of Follow up
    Item
    integer
    C1704685 (UMLS CUI [1,1])
    C0237753 (UMLS CUI [1,2])
    Item Group
    C0031809 (UMLS CUI-1)
    Date of Examination
    Item
    date
    C2826643 (UMLS CUI [1])
    Weight
    Item
    float
    C0005910 (UMLS CUI [1])
    Karnofsky-Index
    Item
    integer
    C0206065 (UMLS CUI [1])
    Item Group
    C0022885 (UMLS CUI-1)
    Date of blood work
    Item
    date
    C0011008 (UMLS CUI [1,1])
    C0005834 (UMLS CUI [1,2])
    Item Group
    C0430022 (UMLS CUI-1)
    CT Abdomen
    Item
    boolean
    C0412620 (UMLS CUI [1])
    Date of CT Abdomen
    Item
    date
    C0011008 (UMLS CUI [1,1])
    C0412620 (UMLS CUI [1,2])
    CT Thorax
    Item
    boolean
    C0202823 (UMLS CUI [1])
    CT Thorax
    Item
    date
    C0011008 (UMLS CUI [1,1])
    C0202823 (UMLS CUI [1,2])
    Echocardiography
    Item
    boolean
    C0013516 (UMLS CUI [1])
    Date of Echocardiography
    Item
    date
    C0011008 (UMLS CUI [1,1])
    C0013516 (UMLS CUI [1,2])
    Item Group
    C0040405 (UMLS CUI-1)
    C1274040 (UMLS CUI-2)
    Aszites
    Item
    boolean
    C0003962 (UMLS CUI [1])
    Metastases
    Item
    boolean
    C3258247 (UMLS CUI [1])
    Peritoneal metastases
    Item
    boolean
    C0346989 (UMLS CUI [1])
    Liver metastases
    Item
    boolean
    C0494165 (UMLS CUI [1])
    Lung metastases
    Item
    boolean
    C0153676 (UMLS CUI [1])
    Bone metastases
    Item
    boolean
    C0153690 (UMLS CUI [1])
    Other metastases
    Item
    text
    C0027627 (UMLS CUI [1,1])
    C0205394 (UMLS CUI [1,2])
    Item Group
    C1707479 (UMLS CUI-1)
    Concomitant therapy
    Item
    boolean
    C1707479 (UMLS CUI [1])
    Tumorspecific therapy
    Item
    boolean
    C1707479 (UMLS CUI [1,1])
    C0006826 (UMLS CUI [1,2])
    C1552740 (UMLS CUI [1,3])
    Complication specific therapy
    Item
    boolean
    C1707479 (UMLS CUI [1,1])
    C0009566 (UMLS CUI [1,2])
    C1552740 (UMLS CUI [1,3])
    Supportive therapy
    Item
    boolean
    C0344211 (UMLS CUI [1,1])
    C1707479 (UMLS CUI [1,2])
    Other therapy
    Item
    text
    C0418967 (UMLS CUI [1,1])
    C1707479 (UMLS CUI [1,2])
    Other therapy
    Item
    boolean
    C0418967 (UMLS CUI [1,1])
    C1707479 (UMLS CUI [1,2])
    Item Group
    C2198186 (UMLS CUI-1)
    Late toxicities
    Item
    boolean
    C2198186 (UMLS CUI [1])
    Item Group
    C2198186 (UMLS CUI-1)
    Ifd. Number
    Item
    integer
    C0237753 (UMLS CUI [1])
    Toxicity
    Item
    text
    C2198186 (UMLS CUI [1])
    Item
    integer
    C2826262 (UMLS CUI [1])
    Toxicity grade
    Code List
    Toxicity grade
    CL Item
     (1)
    CL Item
     (2)
    CL Item
     (3)
    CL Item
     (4)
    CL Item
     (5)
    Item Group
    C0242656 (UMLS CUI-1)
    Item
    text
    C0242656 (UMLS CUI [1,1])
    C0006826 (UMLS CUI [1,2])
    Tumor progress
    Code List
    Tumor progress
    CL Item
     (nein)
    CL Item
     (ja: Progress-Bogen (P) ausfüllen)
    Item Group
    C0877248 (UMLS CUI-1)
    Item
    text
    C0877248 (UMLS CUI [1])
    Adverse Event
    Code List
    Adverse Event
    CL Item
     (ja (AE-Bogen ausfüllen))
    CL Item
     (nein)
    Item
    text
    C0019993 (UMLS CUI [1])
    Hospitalization
    Code List
    Hospitalization
    CL Item
     (ja (HOSP-Bogen ausfüllen))
    CL Item
     (nein)
    Item
    text
    C0549433 (UMLS CUI [1,1])
    C0242656 (UMLS CUI [1,2])
    C0006826 (UMLS CUI [1,3])
    Surgical intervention
    Code List
    Surgical intervention
    CL Item
     (ja (SInt-Bogen ausfüllen))
    CL Item
     (nein)
    Item Group
    Questionnaire
    Item
    boolean
    C0034394 (UMLS CUI [1,1])
    C0205197 (UMLS CUI [1,2])
    C0034380 (UMLS CUI [1,3])
    Questionnaire
    Item
    boolean
    C0034394 (UMLS CUI [1,1])
    C0205197 (UMLS CUI [1,2])
    C0034380 (UMLS CUI [1,3])
    Item Group
    C1320722 (UMLS CUI-1)
    Date
    Item
    date
    C0011008 (UMLS CUI [1])
    Name
    Item
    text
    C0027365 (UMLS CUI [1])
    Signature
    Item
    text
    C1519316 (UMLS CUI [1])
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