Center
Item
Center
text
C1301943 (UMLS CUI [1])
Subject identification - First Name
Item
Subject identification - First Name
text
C1443235 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Subject identification - Family Name
Item
Subject identification - Family Name
text
C1301584 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Date of visit
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Informed Consent Date
Item
Informed Consent Date
date
C0021430 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Is the subject eligible for the study, according to the criteria listed hereby?
Item
Is the subject eligible for the study, according to the criteria listed hereby?
boolean
C0681850 (UMLS CUI [1,1])
C1548635 (UMLS CUI [1,2])
C0243161 (UMLS CUI [2])
If subject is not eligible, please give the corresponding criterion number
Item
If subject is not eligible, please give the corresponding criterion number(s)
text
C0681850 (UMLS CUI [1,1])
C1548635 (UMLS CUI [1,2])
C0243161 (UMLS CUI [2,1])
C0237753 (UMLS CUI [2,2])
Subject initials - First name
Item
Subject initials - First name
text
C2986440 (UMLS CUI [1,1])
C1443235 (UMLS CUI [1,2])
Subject initials - Family name
Item
Subject initials - Family name
text
C2986440 (UMLS CUI [1,1])
C1301584 (UMLS CUI [1,2])
Item
Gender
text
C0079399 (UMLS CUI [1])
Item
Race
text
C0034510 (UMLS CUI [1])
CL Item
Other, please specify (OT)
Other race, please specify
Item
Other race, please specify
text
C0034510 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Height
Item
Height
integer
C0005890 (UMLS CUI [1])
Item
Height unit
integer
C0005890 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Item
Weight unit
integer
C0005910 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Are you aware of any pre-existing conditions or signs and/or symptoms present in the subject prior to the start of the study?
Item
Are you aware of any pre-existing conditions or signs and/or symptoms present in the subject prior to the start of the study?
boolean
C0521987 (UMLS CUI [1,1])
C2603343 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0037088 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
Item
Examination
integer
C0031809 (UMLS CUI [1])
CL Item
Ears-nose-throat (6)
CL Item
Cardiovascular (2)
CL Item
Gastrointestinal (1)
CL Item
Musculoskeletal (7)
CL Item
Genitourinary (12)
CL Item
Other (specify) (99)
Other examination
Item
Other examination
text
C0031809 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Item
Diagnosis status
integer
C0449438 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
Code List
Diagnosis status
Diagnosis
Item
Diagnosis
text
C0011900 (UMLS CUI [1])
Pre- vaccination temperature
Item
Pre- vaccination temperature
float
C0042196 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0005903 (UMLS CUI [2])
Item
Temperature Route
integer
C0005903 (UMLS CUI [1,1])
C0449687 (UMLS CUI [1,2])
Code List
Temperature Route
CL Item
Tympanic oral (3)
CL Item
Tympanic rectal (4)
Has a blood sample been taken?
Item
Has a blood sample been taken?
boolean
C0005834 (UMLS CUI [1])