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ID

31614

Description

Consolidation Whole Abdominal Intensity-Modulated Radiation Therapy (IMRT) in Advanced Ovarian Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01180504 Sponsor: University Hospital Heidelberg Collaborator: Deutsche Krebshilfe e.V., Bonn (Germany) Information provided by: University Hospital Heidelberg Principal Investigator: Andreas Schneeweiss, MD Department of Gyneacology and Obstetrics, Unversity of Heidelberg Principal Investigator: Juergen Debus, MD, PhD Department of Radiation Oncology, University of Heidelberg

Link

https://clinicaltrials.gov/show/NCT01180504

Keywords

Versions (1)
  1. 9/12/18 9/12/18 -
Copyright Holder

Juergen Debus / Prof., M.D., PhD, Department of Radiation Oncology, University of Heidelberg

Uploaded on

September 12, 2018

DOI

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License

Creative Commons BY-NC 3.0
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    Eligibility Ovarian Cancer NCT01180504

    English

    Eligibility Ovarian Cancer NCT01180504

    1 forms  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    histologically confirmed ovarian cancer or tube cancer or primary peritoneal carcinoma stage figo iii
    Description

    Histological confirmation of ovarian cancer or tube cancer or primary peritoneal carcinoma stage figo iii

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0449575
    UMLS CUI [1,2]
    C0029925
    UMLS CUI [1,3]
    C0474956
    UMLS CUI [2,1]
    C0449575
    UMLS CUI [2,2]
    C0153579
    UMLS CUI [2,3]
    C0474956
    UMLS CUI [3,1]
    C0449575
    UMLS CUI [3,2]
    C1514428
    UMLS CUI [3,3]
    C0474956
    primary optimal debulking surgery
    Description

    primary optimal debulking surgery

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1708063
    UMLS CUI [1,2]
    C1706406
    postoperative gross residual tumor ≤ 1cm ( r0, r1 oder r2 < 1cm situation)
    Description

    postoperative gross residual tumor ≤ 1cm

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0475286
    UMLS CUI [1,2]
    C0475440
    adjuvant chemotherapy with platin and taxane
    Description

    adjuvant chemotherapy with platin and taxane

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0085533
    UMLS CUI [1,2]
    C3536920
    UMLS CUI [2,1]
    C0085533
    UMLS CUI [2,2]
    C3541958
    complete remission after chemotherapy
    Description

    complete remission after chemotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0677874
    UMLS CUI [1,2]
    C0392920
    karnofsky performance score > 60
    Description

    Karnofsky performance score

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0206065
    patients >18 years of age
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    written informed consent
    Description

    Written informed consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    stage figo i or ii
    Description

    stage figo i or ii

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0474956
    stage iii with postoperative gross residual tumor > 1cm
    Description

    stage iii with postoperative gross residual tumor > 1cm

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0474956
    UMLS CUI [1,2]
    C0475286
    stage figo iv
    Description

    stage figo iv

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0474956
    recurrence situation
    Description

    Recurrence situation

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0034897
    delayed wound healing post laparotomy
    Description

    delayed wound healing post laparotomy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0151692
    UMLS CUI [1,2]
    C0023038
    leucopenia <2000/ml before radiotherapy
    Description

    Leucopenia <2000/ml before radiotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023530
    thrombocytopenia <75000/ml before radiotherapy
    Description

    Thrombocytopenia <75000/ml before radiotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0040034
    clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease
    Description

    clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0022658
    UMLS CUI [2]
    C0023895
    UMLS CUI [3]
    C0018799
    UMLS CUI [4]
    C0025517
    UMLS CUI [5]
    C0035204
    UMLS CUI [6]
    C0005779
    UMLS CUI [7]
    C1292123
    status post pelvic or abdominal radiotherapy
    Description

    status post pelvic or abdominal radiotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0231290
    UMLS CUI [1,2]
    C1522449
    UMLS CUI [1,3]
    C0030797
    UMLS CUI [2,1]
    C0231290
    UMLS CUI [2,2]
    C1522449
    UMLS CUI [2,3]
    C0000726
    status post other cancer disease in the past 5 years (cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin are excluded)
    Description

    History of other cancer disease in the past 5 years exluding cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2735087
    UMLS CUI [2,1]
    C2828389
    UMLS CUI [2,2]
    C0851140
    UMLS CUI [3,1]
    C2828389
    UMLS CUI [3,2]
    C0007117
    UMLS CUI [4,1]
    C2828389
    UMLS CUI [4,2]
    C0553723
    participation in another clinical trial
    Description

    Participation in another clinical trial

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2348568
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    Similar models

    Eligibility Ovarian Cancer NCT01180504

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Histological confirmation of ovarian cancer or tube cancer or primary peritoneal carcinoma stage figo iii
    Item
    histologically confirmed ovarian cancer or tube cancer or primary peritoneal carcinoma stage figo iii
    boolean
    C0449575 (UMLS CUI [1,1])
    C0029925 (UMLS CUI [1,2])
    C0474956 (UMLS CUI [1,3])
    C0449575 (UMLS CUI [2,1])
    C0153579 (UMLS CUI [2,2])
    C0474956 (UMLS CUI [2,3])
    C0449575 (UMLS CUI [3,1])
    C1514428 (UMLS CUI [3,2])
    C0474956 (UMLS CUI [3,3])
    primary optimal debulking surgery
    Item
    primary optimal debulking surgery
    boolean
    C1708063 (UMLS CUI [1,1])
    C1706406 (UMLS CUI [1,2])
    postoperative gross residual tumor ≤ 1cm
    Item
    postoperative gross residual tumor ≤ 1cm ( r0, r1 oder r2 < 1cm situation)
    boolean
    C0475286 (UMLS CUI [1,1])
    C0475440 (UMLS CUI [1,2])
    adjuvant chemotherapy with platin and taxane
    Item
    adjuvant chemotherapy with platin and taxane
    boolean
    C0085533 (UMLS CUI [1,1])
    C3536920 (UMLS CUI [1,2])
    C0085533 (UMLS CUI [2,1])
    C3541958 (UMLS CUI [2,2])
    complete remission after chemotherapy
    Item
    complete remission after chemotherapy
    boolean
    C0677874 (UMLS CUI [1,1])
    C0392920 (UMLS CUI [1,2])
    Karnofsky performance score
    Item
    karnofsky performance score > 60
    boolean
    C0206065 (UMLS CUI [1])
    Age
    Item
    patients >18 years of age
    boolean
    C0001779 (UMLS CUI [1])
    Written informed consent
    Item
    written informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    stage figo i or ii
    Item
    stage figo i or ii
    boolean
    C0474956 (UMLS CUI [1])
    stage iii with postoperative gross residual tumor > 1cm
    Item
    stage iii with postoperative gross residual tumor > 1cm
    boolean
    C0474956 (UMLS CUI [1,1])
    C0475286 (UMLS CUI [1,2])
    stage figo iv
    Item
    stage figo iv
    boolean
    C0474956 (UMLS CUI [1])
    Recurrence situation
    Item
    recurrence situation
    boolean
    C0034897 (UMLS CUI [1])
    delayed wound healing post laparotomy
    Item
    delayed wound healing post laparotomy
    boolean
    C0151692 (UMLS CUI [1,1])
    C0023038 (UMLS CUI [1,2])
    Leucopenia <2000/ml before radiotherapy
    Item
    leucopenia <2000/ml before radiotherapy
    boolean
    C0023530 (UMLS CUI [1])
    Thrombocytopenia <75000/ml before radiotherapy
    Item
    thrombocytopenia <75000/ml before radiotherapy
    boolean
    C0040034 (UMLS CUI [1])
    clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease
    Item
    clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease
    boolean
    C0022658 (UMLS CUI [1])
    C0023895 (UMLS CUI [2])
    C0018799 (UMLS CUI [3])
    C0025517 (UMLS CUI [4])
    C0035204 (UMLS CUI [5])
    C0005779 (UMLS CUI [6])
    C1292123 (UMLS CUI [7])
    status post pelvic or abdominal radiotherapy
    Item
    status post pelvic or abdominal radiotherapy
    boolean
    C0231290 (UMLS CUI [1,1])
    C1522449 (UMLS CUI [1,2])
    C0030797 (UMLS CUI [1,3])
    C0231290 (UMLS CUI [2,1])
    C1522449 (UMLS CUI [2,2])
    C0000726 (UMLS CUI [2,3])
    History of other cancer disease in the past 5 years exluding cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin
    Item
    status post other cancer disease in the past 5 years (cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin are excluded)
    boolean
    C2735087 (UMLS CUI [1])
    C2828389 (UMLS CUI [2,1])
    C0851140 (UMLS CUI [2,2])
    C2828389 (UMLS CUI [3,1])
    C0007117 (UMLS CUI [3,2])
    C2828389 (UMLS CUI [4,1])
    C0553723 (UMLS CUI [4,2])
    Participation in another clinical trial
    Item
    participation in another clinical trial
    boolean
    C2348568 (UMLS CUI [1])
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