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Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

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An unscheduled PK blood sample must be obtained within 72 hours of last dose
Beschrijving

An unscheduled PK blood sample must be obtained within 72 hours of last dose

1. Was a pharmacokinetic blood sample obtained?
Beschrijving

pharmacokinetic blood sample

Datatype

boolean

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0178913
If yes, date taken
Beschrijving

Date of blood sample

Datatype

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0011008
If yes, time taken
Beschrijving

Time of blood sample

Datatype

time

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0040223
If Yes, date of last investigational product dose prior to PK sample
Beschrijving

date of last investigational product dose prior to PK sample

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0040223
UMLS CUI [1,3]
C0678766
If Yes, time of last investigational product dose prior to PK sample
Beschrijving

time of last investigational product dose prior to PK sample

Datatype

time

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0040223
UMLS CUI [1,3]
C0678766
Sample Identifier/Sample Number
Beschrijving

Sample Identifier and Sample Number are conditional. The study team must choose one for inclusion on the eCRF form.

Datatype

text

Alias
UMLS CUI [1]
C1299222
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Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
An unscheduled PK blood sample must be obtained within 72 hours of last dose
pharmacokinetic blood sample
Item
1. Was a pharmacokinetic blood sample obtained?
boolean
C0031328 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
Date of blood sample
Item
If yes, date taken
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of blood sample
Item
If yes, time taken
time
C0200345 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
date of last investigational product dose prior to PK sample
Item
If Yes, date of last investigational product dose prior to PK sample
date
C0011008 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0678766 (UMLS CUI [1,3])
time of last investigational product dose prior to PK sample
Item
If Yes, time of last investigational product dose prior to PK sample
time
C0011008 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0678766 (UMLS CUI [1,3])
Sample Identifier/Sample Number
Item
Sample Identifier/Sample Number
text
C1299222 (UMLS CUI [1])
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