ID

28277

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

Mots-clés

Versions (2)
  1. 10/12/2017 10/12/2017 -
  2. 02/01/2018 02/01/2018 -
Détendeur de droits

Prof. Dr. med. Georg Heß

Téléchargé le

2 janvier 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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End of study GOAL Trial B-cell Lymphoma NCT02499003

Anglais

End of study GOAL Trial B-cell Lymphoma NCT02499003

1 Formulaires  
End of study
Description

End of study

Alias
UMLS CUI-1
C0008976
UMLS CUI-2
C0444930
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Date of study end
Description

Date of study end

Type de données

date

Alias
UMLS CUI [1]
C2983670
Did the subject complete the follow-up?
Description

follow-up completion

Type de données

boolean

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C0205197
If 'no', please specify reason(s) for early follow-up termination:
Description

termination reason

Type de données

text

Alias
UMLS CUI [1,1]
C1283212
UMLS CUI [1,2]
C0392360
If 'death': Date
Description

Date of death

Type de données

date

Alias
UMLS CUI [1]
C1148348
If 'death': Reason
Description

reason of death

Type de données

text

Alias
UMLS CUI [1]
C0007465
If 'other' reason for early follow-up termination, please specify:
Description

specify

Type de données

text

Alias
UMLS CUI [1]
C1521902
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Similar models

End of study GOAL Trial B-cell Lymphoma NCT02499003

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
End of study
C0008976 (UMLS CUI-1)
C0444930 (UMLS CUI-2)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Date of study end
Item
Date of study end
date
C2983670 (UMLS CUI [1])
follow-up completion
Item
Did the subject complete the follow-up?
boolean
C1522577 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Item
If 'no', please specify reason(s) for early follow-up termination:
text
C1283212 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
early follow-up termination reason
Code List
If 'no', please specify reason(s) for early follow-up termination:
CL Item
Withdrawal of consent (Withdrawal of consent)
C1707492 (UMLS CUI-1)
(Comment:en)
CL Item
Death (Death)
C0011065 (UMLS CUI-1)
(Comment:en)
CL Item
Lost to Follow-Up (Lost to Follow-Up)
C1302313 (UMLS CUI-1)
(Comment:en)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
(Comment:en)
Date of death
Item
If 'death': Date
date
C1148348 (UMLS CUI [1])
Item
If 'death': Reason
text
C0007465 (UMLS CUI [1])
reason of death
Code List
If 'death': Reason
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)
specify
Item
If 'other' reason for early follow-up termination, please specify:
text
C1521902 (UMLS CUI [1])
Retour au début de la page 

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