ID

28248

Descripción

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

Palabras clave

  1. 25/11/17 25/11/17 -
  2. 25/11/17 25/11/17 -
  3. 30/11/17 30/11/17 -
  4. 31/12/17 31/12/17 -
Titular de derechos de autor

Prof. Dr. med. Georg Heß

Subido en

31 de diciembre de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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Screening Informed consent GOAL Trial B-cell Lymphoma NCT02499003

Screening Informed consent GOAL Trial B-cell Lymphoma NCT02499003

Informed consent
Descripción

Informed consent

Alias
UMLS CUI-1
C0021430
Subject ID
Descripción

Subject ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Site No
Descripción

Site Number

Tipo de datos

text

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

Screening number

Tipo de datos

text

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

Informed consent availability

Tipo de datos

boolean

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

Date of informed consent

Tipo de datos

date

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

Study subject participation status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Screening Informed consent GOAL Trial B-cell Lymphoma NCT02499003

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])

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