ID

28330

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: Investigational product (Liver)

Stichworte

Versionen (5)
  1. 11.10.17 11.10.17 -
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  3. 16.10.17 16.10.17 -
  4. 23.10.17 23.10.17 -
  5. 04.01.18 04.01.18 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

4. Januar 2018

DOI

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Lizenz

Creative Commons BY-NC 3.0
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Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

Englisch

Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare  
If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.
Beschreibung

If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.

1. Start Date Investigational Product [-99]
Beschreibung

Start Date Investigational Product treatment period

Datentyp

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
1. Start Date Investigational Product not applicable [-98]
Beschreibung

Start Date Investigational Product treatment period not applicable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1272460
2. End Date Investigational Product [-99]
Beschreibung

End Date Investigational Product treatment period

Datentyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
2. End Date Investigational Product not applicable [-98]
Beschreibung

End Date Investigational Product treatment period not applicable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
UMLS CUI [1,3]
C1272460
If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.
Beschreibung

If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.

3. Start Date Investigational Product [-99]
Beschreibung

Start Date Investigational Product

Datentyp

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
3. Start Date Investigational Product not applicable [-98]
Beschreibung

Start Date Investigational Product not applicable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1272460
4. End Date Investigational Product [-99]
Beschreibung

End Date Investigational Product

Datentyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
4. End Date Investigational Product not applicable [-98]
Beschreibung

End Date Investigational Product not applicable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
UMLS CUI [1,3]
C1272460
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Ähnliche Modelle

Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.
Start Date Investigational Product treatment period
Item
1. Start Date Investigational Product [-99]
date
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date Investigational Product treatment period not applicable
Item
1. Start Date Investigational Product not applicable [-98]
boolean
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
End Date Investigational Product treatment period
Item
2. End Date Investigational Product [-99]
date
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
End Date Investigational Product treatment period not applicable
Item
2. End Date Investigational Product not applicable [-98]
boolean
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
Item Group
If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.
Start Date Investigational Product
Item
3. Start Date Investigational Product [-99]
date
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date Investigational Product not applicable
Item
3. Start Date Investigational Product not applicable [-98]
boolean
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
End Date Investigational Product
Item
4. End Date Investigational Product [-99]
date
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
End Date Investigational Product not applicable
Item
4. End Date Investigational Product not applicable [-98]
boolean
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
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