ID

27862

Description

Study part: Concomitant Medication. A Randomized Phase II Trial of Transarterial Radioembolisation With Yttrium-90 (SIRT) in Comparison to Transarterial Chemoembolisation With Cisplatin (TACE) in Patients With Liver Metastases From Uveal Melanoma. Provided by Prof. Dr. Ulrich Keilholz, Charité – University of medicine Berlin. EudraCT-Nummer: 2014-002439-32. NCT02936388.

Keywords

  1. 12/3/17 12/3/17 -
Copyright Holder

Charité – University of medicine Berlin

Uploaded on

December 3, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Concomitant Medication SirTac NCT02936388

Concomitant Medication

  1. StudyEvent: ODM
    1. Concomitant Medication
Begleitmedikation
Description

Begleitmedikation

Alias
UMLS CUI-1
C2347852
Patienten-ID:
Description

Patienten-ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Random. Nr.:
Description

Random. Nr.

Data type

text

Alias
UMLS CUI [1,1]
C1300638
UMLS CUI [1,2]
C0034656
Medikamente
Description

medication name

Data type

text

Alias
UMLS CUI [1]
C2360065
Applikation
Description

drug administration route

Data type

text

Alias
UMLS CUI [1]
C0013153
Dosis inklusiv Einheit
Description

dosage

Data type

text

Alias
UMLS CUI [1]
C0178602
Grund der Einnahme
Description

Indication

Data type

text

Alias
UMLS CUI [1]
C3146298
Stardatum
Description

start date

Data type

date

Alias
UMLS CUI [1]
C0808070
Stopdatum
Description

stop date

Data type

date

Alias
UMLS CUI [1]
C0806020
Andauernd
Description

ongoing

Data type

boolean

Alias
UMLS CUI [1]
C2826666
Ausgefüllt/bestätigt am:
Description

date

Data type

date

Alias
UMLS CUI [1]
C0011008
Name Prüfarzt
Description

investigator name

Data type

text

Alias
UMLS CUI [1]
C2826892
Unterschrift Prüfarzt
Description

investigator signature

Data type

text

Alias
UMLS CUI [1]
C2346576

Similar models

Concomitant Medication

  1. StudyEvent: ODM
    1. Concomitant Medication
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Begleitmedikation
C2347852 (UMLS CUI-1)
Patienten-ID
Item
Patienten-ID:
text
C2348585 (UMLS CUI [1])
Random. Nr.
Item
Random. Nr.:
text
C1300638 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
medication name
Item
Medikamente
text
C2360065 (UMLS CUI [1])
Item
Applikation
text
C0013153 (UMLS CUI [1])
Code List
Applikation
CL Item
oral  (1)
CL Item
i.v. (2)
CL Item
i.m. (3)
CL Item
s.c. (4)
CL Item
rektal (5)
CL Item
dermal (6)
CL Item
Inhalation (7)
CL Item
andere (8)
dosage
Item
Dosis inklusiv Einheit
text
C0178602 (UMLS CUI [1])
Indication
Item
Grund der Einnahme
text
C3146298 (UMLS CUI [1])
start date
Item
Stardatum
date
C0808070 (UMLS CUI [1])
stop date
Item
Stopdatum
date
C0806020 (UMLS CUI [1])
ongoing
Item
Andauernd
boolean
C2826666 (UMLS CUI [1])
date
Item
Ausgefüllt/bestätigt am:
date
C0011008 (UMLS CUI [1])
investigator name
Item
Name Prüfarzt
text
C2826892 (UMLS CUI [1])
investigator signature
Item
Unterschrift Prüfarzt
text
C2346576 (UMLS CUI [1])

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