ID

28275

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

Keywords

  1. 12/7/17 12/7/17 -
  2. 1/2/18 1/2/18 -
Copyright Holder

Prof. Dr. med. Georg Heß

Uploaded on

January 2, 2018

DOI

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License

Creative Commons BY-NC 3.0

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Concomitant Medication GOAL Trial B-cell Lymphoma NCT02499003

Concomitant Medication GOAL Trial B-cell Lymphoma NCT02499003

Admininstrative data
Description

Admininstrative data

Alias
UMLS CUI-1
C1320722
Subject ID
Description

Subject ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Are there any relevant concomitant medications (incl. all transfusion packs)?
Description

concomitant medications

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Concomitant Medication
Description

Concomitant Medication

Alias
UMLS CUI-1
C2347852
No.
Description

medication number

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0449788
Medication
Description

Medication

Data type

text

Alias
UMLS CUI [1]
C0013227
Indication
Description

Indication

Data type

text

Alias
UMLS CUI [1]
C3146298
Dose Unit [e .g. 10, as needed]
Description

Dose Unit

Data type

text

Alias
UMLS CUI [1]
C0869039
Dose form
Description

Dose form

Data type

integer

Alias
UMLS CUI [1]
C0013058
Start date
Description

Start date

Data type

date

Alias
UMLS CUI [1]
C0808070
Stop date
Description

Stop date

Data type

date

Alias
UMLS CUI [1]
C0806020
Ongoing at End of Treatment?
Description

Ongoing medication End of Treatment

Data type

boolean

Alias
UMLS CUI [1]
C2826666

Similar models

Concomitant Medication GOAL Trial B-cell Lymphoma NCT02499003

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Admininstrative data
C1320722 (UMLS CUI-1)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
concomitant medications
Item
Are there any relevant concomitant medications (incl. all transfusion packs)?
boolean
C2347852 (UMLS CUI [1])
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
medication number
Item
No.
integer
C0013227 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Medication
Item
Medication
text
C0013227 (UMLS CUI [1])
Indication
Item
Indication
text
C3146298 (UMLS CUI [1])
Dose Unit
Item
Dose Unit [e .g. 10, as needed]
text
C0869039 (UMLS CUI [1])
Item
Dose form
integer
C0013058 (UMLS CUI [1])
Code List
Dose form
CL Item
Tablet (0)
C0039225 (UMLS CUI-1)
(Comment:en)
CL Item
Film-coated tablet (1)
C1273643 (UMLS CUI-1)
(Comment:en)
CL Item
Chewable tablet (2)
C0304290 (UMLS CUI-1)
(Comment:en)
CL Item
Throat lozenge (3)
C0784478 (UMLS CUI-1)
(Comment:en)
CL Item
Capsule (4)
C0006935 (UMLS CUI-1)
(Comment:en)
CL Item
Dragee (5)
(Comment:en)
CL Item
Powder (6)
C0991575 (UMLS CUI-1)
(Comment:en)
CL Item
Granulate (7)
(Comment:en)
CL Item
Salve (8)
C1710011 (UMLS CUI-1)
(Comment:en)
CL Item
Cream (9)
C0028912 (UMLS CUI-1)
(Comment:en)
CL Item
Drop (10)
CL Item
Spray (11)
CL Item
Solution (12)
CL Item
Injection (13)
CL Item
Infusion (14)
CL Item
Adhesive Bandage (15)
CL Item
Juice (16)
CL Item
Sachets (17)
CL Item
Gel (18)
CL Item
Suppository (19)
CL Item
Carbon tablets (20)
CL Item
Inhalant (21)
Start date
Item
Start date
date
C0808070 (UMLS CUI [1])
Stop date
Item
Stop date
date
C0806020 (UMLS CUI [1])
Ongoing medication End of Treatment
Item
Ongoing at End of Treatment?
boolean
C2826666 (UMLS CUI [1])

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