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

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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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