ID

28336

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

Mots-clés

  1. 2017-11-30 2017-11-30 -
  2. 2018-01-04 2018-01-04 -
Détendeur de droits

Prof. Dr. med. Georg Heß

Téléchargé le

4 januari 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :


Aucun commentaire

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Screening Registration GOAL Trial B-cell Lymphoma NCT02499003

Screening Registration GOAL Trial B-cell Lymphoma NCT02499003

Admininstrative data
Description

Admininstrative data

Alias
UMLS CUI-1
C1320722
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Registration
Description

Registration

Alias
UMLS CUI-1
C1514821
Subject complies with all inclusion criteria?
Description

compliance inclusion criteria

Type de données

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C1512693
Subject complies with all exclusion criteria?
Description

compliance exclusion criteria

Type de données

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0680251
Include subject into study?
Description

In case of non-inclusion, please fill out the End of Study form

Type de données

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C2348563
Patient No.
Description

Patient number

Type de données

integer

Alias
UMLS CUI [1]
C1830427

Similar models

Screening Registration GOAL Trial B-cell Lymphoma NCT02499003

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Admininstrative data
C1320722 (UMLS CUI-1)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Item Group
Registration
C1514821 (UMLS CUI-1)
compliance inclusion criteria
Item
Subject complies with all inclusion criteria?
boolean
C1321605 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
compliance exclusion criteria
Item
Subject complies with all exclusion criteria?
boolean
C1321605 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Inclusion in study
Item
Include subject into study?
boolean
C1512693 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Patient number
Item
Patient No.
integer
C1830427 (UMLS CUI [1])

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial