First registration (DKKR)

  1. StudyEvent: ODM-Test
    1. First registration (DKKR)
Default Itemgroup
Descripción

Default Itemgroup

Alias
UMLS CUI-1
C1320722
Patient ID
Descripción

Default item

Tipo de datos

text

Alias
UMLS CUI-1
C1549740
Hospital address
Tipo de datos

text

Alias
UMLS CUI-1
C2986046
Hospital telephone
Tipo de datos

text

Alias
UMLS CUI-1
C2986429
Patient surname
Tipo de datos

text

Alias
UMLS CUI-1
C0421448
Patient first name
Tipo de datos

text

Alias
UMLS CUI-1
C0421447
Date of Birth
Tipo de datos

date

Alias
UMLS CUI-1
C0421451
Geschlecht
Descripción

Gender

Tipo de datos

integer

Alias
UMLS CUI-1
C0079399
Country of residence Germany at disease onset
Tipo de datos

boolean

Patient address
Tipo de datos

text

Alias
UMLS CUI-1
C0421449
Birth place
Tipo de datos

text

Alias
UMLS CUI-1
C0032040
Patient ID
Tipo de datos

text

Alias
UMLS CUI-1
C1549740
Diagnosis
Tipo de datos

text

Alias
UMLS CUI-1
C0011900
Localization
Tipo de datos

text

Alias
UMLS CUI-1
C0475264
Stage
Tipo de datos

text

Alias
UMLS CUI-1
C0449394
Grading
Tipo de datos

text

Alias
UMLS CUI-1
C0919553
Diagnosis date
Tipo de datos

date

Alias
UMLS CUI-1
C2316983
Procedure aiding diagnosis
Tipo de datos

integer

Alias
UMLS CUI-1
C0430008
Side
Tipo de datos

integer

Alias
UMLS CUI-1
C0441987
Study Name
Tipo de datos

text

Alias
UMLS CUI-1
C2348560
Written consent
Tipo de datos

text

Alias
UMLS CUI-1
C0021430
Patient given information
Tipo de datos

boolean

Alias
UMLS CUI-1
C0522479
Physician
Tipo de datos

text

Alias
UMLS CUI-1
C0031831
Date
Tipo de datos

date

Alias
UMLS CUI-1
C0011008
Signature
Tipo de datos

text

Alias
UMLS CUI-1
C1519316

Similar models

First registration (DKKR)

  1. StudyEvent: ODM-Test
    1. First registration (DKKR)
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Default Itemgroup
C1320722 (UMLS CUI-1)
Patient ID
Item
text
C1549740 (UMLS CUI-1)
Hospital address
Item
text
C2986046 (UMLS CUI-1)
Hospital telephone
Item
text
C2986429 (UMLS CUI-1)
Patient surname
Item
text
C0421448 (UMLS CUI-1)
Patient first name
Item
text
C0421447 (UMLS CUI-1)
Date of Birth
Item
date
C0421451 (UMLS CUI-1)
Item
Geschlecht
integer
C0079399 (UMLS CUI-1)
Code List
Geschlecht
CL Item
male (1)
C0024554 (UMLS CUI-1)
CL Item
female (2)
C0015780 (UMLS CUI-1)
Country of residence Germany at disease onset
Item
boolean
Patient address
Item
text
C0421449 (UMLS CUI-1)
Birth place
Item
text
C0032040 (UMLS CUI-1)
Patient ID
Item
text
C1549740 (UMLS CUI-1)
Diagnosis
Item
text
C0011900 (UMLS CUI-1)
Localization
Item
text
C0475264 (UMLS CUI-1)
Stage
Item
text
C0449394 (UMLS CUI-1)
Grading
Item
text
C0919553 (UMLS CUI-1)
Diagnosis date
Item
date
C2316983 (UMLS CUI-1)
Item
integer
C0430008 (UMLS CUI-1)
Code List
Procedure aiding diagnosis
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
CL Item
 (5)
CL Item
 (6)
Item
integer
C0441987 (UMLS CUI-1)
Code List
Side
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
CL Item
 (5)
CL Item
 (6)
Study Name
Item
text
C2348560 (UMLS CUI-1)
Item
text
C0021430 (UMLS CUI-1)
Code List
Written consent
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
Patient given information
Item
boolean
C0522479 (UMLS CUI-1)
Physician
Item
text
C0031831 (UMLS CUI-1)
Date
Item
date
C0011008 (UMLS CUI-1)
Signature
Item
text
C1519316 (UMLS CUI-1)