ID

28248

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. Study part: Informed consent (Screening) Source: Prof. Dr. med. Georg Heß Universitätsmedizin Mainz

Mots-clés

  1. 25/11/2017 25/11/2017 -
  2. 25/11/2017 25/11/2017 -
  3. 30/11/2017 30/11/2017 -
  4. 31/12/2017 31/12/2017 -
Détendeur de droits

Prof. Dr. med. Georg Heß

Téléchargé le

31 décembre 2017

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 :

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

Screening Informed consent GOAL Trial B-cell Lymphoma NCT02499003

Screening Informed consent GOAL Trial B-cell Lymphoma NCT02499003

Informed consent
Description

Informed consent

Alias
UMLS CUI-1
C0021430
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Site No
Description

Site Number

Type de données

text

Alias
UMLS CUI [1,1]
C0018704
UMLS CUI [1,2]
C0600091
Screening no
Description

Screening number

Type de données

text

Alias
UMLS CUI [1]
C1710477
Signed and dated informed consent of the patient is available before start of any trial specific procedures
Description

Informed consent availability

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0470187
Date of informed consent
Description

Date of informed consent

Type de données

date

Alias
UMLS CUI [1]
C2985782
Participation in contributing scientific investigations
Description

Study subject participation status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Screening Informed consent GOAL Trial B-cell Lymphoma NCT02499003

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Informed consent
C0021430 (UMLS CUI-1)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Site Number
Item
Site No
text
C0018704 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Screening number
Item
Screening no
text
C1710477 (UMLS CUI [1])
Informed consent availability
Item
Signed and dated informed consent of the patient is available before start of any trial specific procedures
boolean
C0021430 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
Date of informed consent
Item
Date of informed consent
date
C2985782 (UMLS CUI [1])
Study subject participation status
Item
Participation in contributing scientific investigations
boolean
C2348568 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

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