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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