ID

28311

Beschreibung

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Pharmacokinetics - Repeating form (Scheduled visits)

Stichworte

  1. 05.10.17 05.10.17 -
  2. 16.10.17 16.10.17 -
  3. 23.10.17 23.10.17 -
  4. 03.01.18 03.01.18 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

3. Januar 2018

DOI

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Creative Commons BY-NC 3.0

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Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

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

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

1. Was a pharmacokinetic blood sample obtained?
Beschreibung

pharmacokinetic blood sample

Datentyp

boolean

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

Date of blood sample

Datentyp

date

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

Time of blood sample

Datentyp

time

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

date of last investigational product dose prior to PK sample

Datentyp

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
Beschreibung

time of last investigational product dose prior to PK sample

Datentyp

time

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

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

Datentyp

text

Alias
UMLS CUI [1]
C1299222

Ähnliche Modelle

Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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