Follow- Up

  1. StudyEvent: ODM
    1. Follow- Up
Follow- Up
Description

Follow- Up

Alias
UMLS CUI-1
C1522577
Patienten-ID:
Description

Patient-ID

Data type

text

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

randomization number

Data type

text

Alias
UMLS CUI [1,1]
C1300638
UMLS CUI [1,2]
C0034656
Follow-up Visite Nr.:
Description

visit number

Data type

integer

Alias
UMLS CUI [1]
C1549755
Durchgeführt am
Description

visit date

Data type

date

Alias
UMLS CUI [1]
C1320303
Allgemeiner Zustand:
Description

general condition

Data type

text

Alias
UMLS CUI [1]
C1142435
Krankheitsverlauf (Folgetherapien, relevante Ereignisse usw.):
Description

course of a disease

Data type

text

Alias
UMLS CUI [1]
C0242656
Späte Toxizitäten:
Description

Späte Toxizitäten:

Alias
UMLS CUI-1
C0013221
Code
Description

laut CTCAE-Kriterien

Data type

text

Alias
UMLS CUI [1]
C0805701
Art der Toxizität
Description

drug toxicity

Data type

text

Alias
UMLS CUI [1]
C0013221
Grad
Description

laut CTCAE-Kriterien

Data type

text

Alias
UMLS CUI [1,1]
C0441800
UMLS CUI [1,2]
C0013221
Keine Toxizität zu dokumentieren
Description

Documentation drug toxicity

Data type

boolean

Alias
UMLS CUI [1,1]
C0920316
UMLS CUI [1,2]
C0013221
Kommentar:
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
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

Follow- Up

  1. StudyEvent: ODM
    1. Follow- Up
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Follow- Up
C1522577 (UMLS CUI-1)
Patient-ID
Item
Patienten-ID:
text
C2348585 (UMLS CUI [1])
randomization number
Item
Random. Nr.:
text
C1300638 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
visit number
Item
Follow-up Visite Nr.:
integer
C1549755 (UMLS CUI [1])
visit date
Item
Durchgeführt am
date
C1320303 (UMLS CUI [1])
general condition
Item
Allgemeiner Zustand:
text
C1142435 (UMLS CUI [1])
course of a disease
Item
Krankheitsverlauf (Folgetherapien, relevante Ereignisse usw.):
text
C0242656 (UMLS CUI [1])
Item Group
Späte Toxizitäten:
C0013221 (UMLS CUI-1)
Code
Item
Code
text
C0805701 (UMLS CUI [1])
drug toxicity
Item
Art der Toxizität
text
C0013221 (UMLS CUI [1])
Grade drug toxicity
Item
Grad
text
C0441800 (UMLS CUI [1,1])
C0013221 (UMLS CUI [1,2])
Documentation drug toxicity
Item
Keine Toxizität zu dokumentieren
boolean
C0920316 (UMLS CUI [1,1])
C0013221 (UMLS CUI [1,2])
comment
Item
Kommentar:
text
C0947611 (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])