ID

28021

Beschreibung

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. Visit: All visits. Source: Prof. Dr. med. Georg Heß Universitätsmedizin Mainz

Stichworte

  1. 10.12.17 10.12.17 -
  2. 02.01.18 02.01.18 -
Rechteinhaber

Prof. Dr. med. Georg Heß

Hochgeladen am

10. Dezember 2017

DOI

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Lizenz

Creative Commons BY-NC 3.0

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Adverse events GOAL Trial B-cell Lymphoma NCT02499003

Adverse events GOAL Trial B-cell Lymphoma NCT02499003

Admininstrative data
Beschreibung

Admininstrative data

Subject ID
Beschreibung

Subject ID

Datentyp

text

Alias
UMLS CUI [1]
C2348585
Page
Beschreibung

Page

Datentyp

integer

Adverse events
Beschreibung

Adverse events

No.
Beschreibung

adverse event number

Datentyp

integer

AE Term (based on CTCAE 4.0)
Beschreibung

Adverse event

Datentyp

text

SAE?
Beschreibung

Serious adverse event

Datentyp

text

Study termination
Beschreibung

Study termination

Datentyp

text

Start date
Beschreibung

Start date

Datentyp

date

Stop date
Beschreibung

Stop date

Datentyp

date

Ongoing at End of Treatment?
Beschreibung

Ongoing adverse event at End of Treatment

Datentyp

boolean

Max. CTCAE grade
Beschreibung

Maximum CTCAE grade

Datentyp

integer

Causality with Obinutuzumab
Beschreibung

Causality with Obinutuzumab

Datentyp

integer

Causality with Pixantrone
Beschreibung

Causality with Pixantrone

Datentyp

integer

Action taken with Obinutuzumab
Beschreibung

Action taken with Obinutuzumab

Datentyp

integer

Action taken with Pixantrone
Beschreibung

Action taken with Pixantrone

Datentyp

integer

Treatment given?
Beschreibung

Treatment

Datentyp

text

Outcome
Beschreibung

Treatment Outcome

Datentyp

integer

I have reviewed the AEs on this page and have assessed them for seriousness, causality, severity and outcome and confirm that, to the best of my knowledge, they accurately reflect the study information obtained for this patient.
Beschreibung

I have reviewed the AEs on this page and have assessed them for seriousness, causality, severity and outcome and confirm that, to the best of my knowledge, they accurately reflect the study information obtained for this patient.

Data correct?
Beschreibung

Data correct

Datentyp

boolean

Date of signature
Beschreibung

Date of signature

Datentyp

date

Name of investigator
Beschreibung

Name of investigator

Datentyp

text

Ähnliche Modelle

Adverse events GOAL Trial B-cell Lymphoma NCT02499003

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Admininstrative data
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Page
Item
Page
integer
Item Group
Adverse events
Item
No.
integer
CL Item
01 (1)
CL Item
02 (2)
CL Item
03 (3)
CL Item
04 (4)
CL Item
05 (5)
CL Item
06 (6)
CL Item
07 (7)
CL Item
08 (8)
CL Item
09 (9)
CL Item
10 (10)
Adverse event
Item
AE Term (based on CTCAE 4.0)
text
CL Item
Yes (Y)
CL Item
No (N)
Item
Study termination
text
Code List
Study termination
CL Item
Yes (Y)
CL Item
No (N)
Start date
Item
Start date
date
Stop date
Item
Stop date
date
Ongoing adverse event at End of Treatment
Item
Ongoing at End of Treatment?
boolean
Maximum CTCAE grade
Item
Max. CTCAE grade
integer
Item
Causality with Obinutuzumab
integer
Code List
Causality with Obinutuzumab
CL Item
Not related (1)
CL Item
Related (2)
Item
Causality with Pixantrone
integer
Code List
Causality with Pixantrone
CL Item
Not related (1)
CL Item
Related (2)
Item
Action taken with Obinutuzumab
integer
Code List
Action taken with Obinutuzumab
CL Item
Unchanged (1)
CL Item
Reduced (2)
CL Item
Interrupted (3)
CL Item
Discontinued (4)
CL Item
Not applicable (5)
Item
Action taken with Pixantrone
integer
Code List
Action taken with Pixantrone
CL Item
Unchanged (1)
CL Item
Reduced (2)
CL Item
Interrupted (3)
CL Item
Discontinued (4)
CL Item
Not applicable (5)
Item
Treatment given?
text
Code List
Treatment given?
CL Item
Yes (Y)
CL Item
No (N)
Item
Outcome
integer
Code List
Outcome
CL Item
Recovered (1)
CL Item
Recovered with sequelae (2)
CL Item
Recovering (3)
CL Item
Not recovered (4)
CL Item
Fatal (5)
CL Item
Unknown (6)
Item Group
I have reviewed the AEs on this page and have assessed them for seriousness, causality, severity and outcome and confirm that, to the best of my knowledge, they accurately reflect the study information obtained for this patient.
Data correct
Item
Data correct?
boolean
Date of signature
Item
Date of signature
date
Name of investigator
Item
Name of investigator
text

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