ID

28250

Description

NCT02499003 The GOAL Trial: Rescue Treatment With the Monoclonal Anti CD20-antibody Obinutuzumab (GA101) in Combination With Pixantrone for the Treatment of Patients With Relapsed Aggressive B-cell Lymphoma Source: Prof. Dr. med. Georg Heß Universitätsmedizin Mainz

Keywords

Versions (2)
  1. 12/7/17 12/7/17 -
  2. 12/31/17 12/31/17 -
Copyright Holder

Prof. Dr. med. Georg Heß

Uploaded on

December 31, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Patient Status GOAL Trial B-cell Lymphoma NCT02499003

English

Patient Status GOAL Trial B-cell Lymphoma NCT02499003

1 forms  
Administrative data
Description

Administrative data

Alias
UMLS CUI-1
C1320722
Subject ID
Description

Subject ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Visit
Description

Visit

Data type

text

Alias
UMLS CUI [1]
C0545082
Patient status
Description

Patient status

Alias
UMLS CUI-1
C0449437
Patient status
Description

Patient status

Data type

text

Alias
UMLS CUI [1]
C0449437
If 'Patient alive':
Description

If 'Patient alive':

Alias
UMLS CUI-1
C3846084
Date of follow up
Description

Date of follow up

Data type

date

Alias
UMLS CUI [1]
C3694716
Progression after last contact?
Description

Disease Progression

Data type

text

Alias
UMLS CUI [1]
C0242656
If 'YES': Date of diagnosis of progression
Description

Date of diagnosis Disease Progression

Data type

date

Alias
UMLS CUI [1,1]
C2316983
UMLS CUI [1,2]
C0242656
Diagnosis via
Description

Method of Diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0332307
UMLS CUI [1,2]
C0449851
UMLS CUI [1,3]
C0011900
If 'Other', please specify:
Description

other

Data type

text

Alias
UMLS CUI [1]
C0205394
If 'Patient deceased':
Description

If 'Patient deceased':

Alias
UMLS CUI-1
C1555024
Date of death
Description

Date of death

Data type

date

Alias
UMLS CUI [1]
C1148348
Cause of death
Description

Cause of death

Data type

text

Alias
UMLS CUI [1]
C0007465
If 'other', please specify:
Description

other

Data type

text

Alias
UMLS CUI [1]
C0205394
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Similar models

Patient Status GOAL Trial B-cell Lymphoma NCT02499003

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Item
Visit
text
C0545082 (UMLS CUI [1])
Visit
Code List
Visit
CL Item
Follow Up 1 (Follow Up 1)
CL Item
Follow Up 2 (Follow Up 2)
CL Item
Follow Up 3 (Follow Up 3)
CL Item
Follow Up 4 (Follow Up 4)
CL Item
Follow Up 5 (Follow Up 5)
CL Item
Follow Up 6 (Follow Up 6)
CL Item
Follow Up 7 (Follow Up 7)
CL Item
Follow Up 8 (Follow Up 8)
CL Item
Follow Up 9 (Follow Up 9)
Item Group
Patient status
C0449437 (UMLS CUI-1)
Item
Patient status
text
C0449437 (UMLS CUI [1])
Patient status
Code List
Patient status
CL Item
Patient alive (Patient alive)
C3846084 (UMLS CUI-1)
(Comment:en)
CL Item
Patient deceased (Patient deceased)
C1555024 (UMLS CUI-1)
(Comment:en)
CL Item
Lost-to-follow-up (Lost-to-follow-up)
C1302313 (UMLS CUI-1)
(Comment:en)
CL Item
Follow-up not done (Follow-up not done)
C0589120 (UMLS CUI-1)
(Comment:en)
Item Group
If 'Patient alive':
C3846084 (UMLS CUI-1)
Date of follow up
Item
Date of follow up
date
C3694716 (UMLS CUI [1])
Item
Progression after last contact?
text
C0242656 (UMLS CUI [1])
Progression after last contact
Code List
Progression after last contact?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Diagnostics not done) (Unknown (Diagnostics not done))
Date of diagnosis Disease Progression
Item
If 'YES': Date of diagnosis of progression
date
C2316983 (UMLS CUI [1,1])
C0242656 (UMLS CUI [1,2])
Item
Diagnosis via
text
C0332307 (UMLS CUI [1,1])
C0449851 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
Means of diagnosis
Code List
Diagnosis via
CL Item
CT (CT)
C0040405 (UMLS CUI-1)
(Comment:en)
CL Item
MRI (MRI)
C0024485 (UMLS CUI-1)
(Comment:en)
CL Item
Clinically evident (Clinically evident)
C2826634 (UMLS CUI-1)
(Comment:en)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
(Comment:en)
other
Item
If 'Other', please specify:
text
C0205394 (UMLS CUI [1])
Item Group
If 'Patient deceased':
C1555024 (UMLS CUI-1)
Date of death
Item
Date of death
date
C1148348 (UMLS CUI [1])
Item
Cause of death
text
C0007465 (UMLS CUI [1])
Cause of death
Code List
Cause of death
CL Item
Progression of underlying disease (Progression of underlying disease)
C0242656 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (Unknown)
C0439673 (UMLS CUI-1)
(Comment:en)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
(Comment:en)
other
Item
If 'other', please specify:
text
C0205394 (UMLS CUI [1])
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