Concomitant Vaccination

Administrative data
Description

Administrative data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Description

Clinical Trial Subject Unique Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
Cohort
Description

Cohort

Data type

integer

Alias
UMLS CUI [1]
C0599755
Visit Type
Description

Visit Type

Data type

integer

Alias
UMLS CUI [1,1]
C0332307
UMLS CUI [1,2]
C0545082
Date of Visit
Description

Date of Visit

Data type

date

Alias
UMLS CUI [1]
C1320303
Concomitant Vaccination
Description

Concomitant Vaccination

Alias
UMLS CUI-1
C0042196
UMLS CUI-2
C2347852
Have any vaccines other than the study vaccine(s) been administered during the timeframe as specified in the Protocol?
Description

Any vaccine not foreseen in the study protocol administered during the period beginning 30 days preceding the first dose of the study vaccines and during the entire study period is to be recorded in this “concomitant medication/vaccination” form with trade name and/or generic name, route of administration and date(s) of administration. If yes, fill in the itemgroup below or each vaccine.

Data type

boolean

Alias
UMLS CUI [1,1]
C0042196
UMLS CUI [1,2]
C2347852
UMLS CUI [1,3]
C0347984
UMLS CUI [1,4]
C1948053
UMLS CUI [1,5]
C2348563
Concomitant Vaccination Details
Description

Concomitant Vaccination Details

Alias
UMLS CUI-1
C0042196
UMLS CUI-2
C2347852
UMLS CUI-3
C2348235
Vaccination Trade Name/ (Generic) Name
Description

Vaccination Trade Name/ (Generic) Name

Data type

text

Alias
UMLS CUI [1,1]
C0042196
UMLS CUI [1,2]
C2360065
UMLS CUI [2,1]
C0042196
UMLS CUI [2,2]
C0592502
Vaccination Administration Route
Description

Vaccination Administration Route

Data type

text

Alias
UMLS CUI [1,1]
C0013153
UMLS CUI [1,2]
C0042196
Vaccination Administration Date
Description

Vaccination Administration Date

Data type

date

Alias
UMLS CUI [1,1]
C1533734
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0042196
Sponsor Comment
Description

(for GSK)

Data type

text

Alias
UMLS CUI [1,1]
C0947611
UMLS CUI [1,2]
C2347796

Similar models

Concomitant Vaccination

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item
Cohort
integer
C0599755 (UMLS CUI [1])
Code List
Cohort
CL Item
HIV-pos. (1)
CL Item
HIV-neg. exposed (2)
CL Item
HIV-neg. unexposed, 3+1 schedule (3)
CL Item
HIV-neg. unexposed, 3+0 schedule (4)
CL Item
HIV-neg. unexposed, 2+1 schedule (5)
Item
Visit Type
integer
C0332307 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
Code List
Visit Type
CL Item
Interim Analysis at/after Visit 6 (1)
CL Item
End of Study Analysis at/after Visit 10 (2)
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Item Group
Concomitant Vaccination
C0042196 (UMLS CUI-1)
C2347852 (UMLS CUI-2)
Concomitant vaccines during protocol-specified period?
Item
Have any vaccines other than the study vaccine(s) been administered during the timeframe as specified in the Protocol?
boolean
C0042196 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C1948053 (UMLS CUI [1,4])
C2348563 (UMLS CUI [1,5])
Item Group
Concomitant Vaccination Details
C0042196 (UMLS CUI-1)
C2347852 (UMLS CUI-2)
C2348235 (UMLS CUI-3)
Vaccination Trade Name/ (Generic) Name
Item
Vaccination Trade Name/ (Generic) Name
text
C0042196 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
C0042196 (UMLS CUI [2,1])
C0592502 (UMLS CUI [2,2])
Item
Vaccination Administration Route
text
C0013153 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
Code List
Vaccination Administration Route
CL Item
Intradermal  (ID)
CL Item
Inhalation  (IH)
CL Item
Intramuscular  (IM)
CL Item
Intravenous  (IV)
CL Item
Other  (OTH)
CL Item
Parenteral  (PE)
CL Item
Oral  (PO)
CL Item
Subcutaneous  (SC)
CL Item
Sublingual  (SL)
CL Item
Transdermal  (TD)
CL Item
Unknown  (UNK)
CL Item
Intranasal  (IN)
Vaccination Administration Date
Item
Vaccination Administration Date
date
C1533734 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0042196 (UMLS CUI [1,3])
Sponsor Comment
Item
Sponsor Comment
text
C0947611 (UMLS CUI [1,1])
C2347796 (UMLS CUI [1,2])