ID
28403
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: CEC -revascularisation Repeating form (Scheduled visits)
Stichworte
Versionen (3)
- 11.10.17 11.10.17 -
- 23.10.17 23.10.17 -
- 11.01.18 11.01.18 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
11. Januar 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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CEC - revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
CEC - revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
Beschreibung
Urgent coronary revascularisation for myocardial ischemia
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C0680730
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0151744
- UMLS CUI [1,2]
- C0948089
Beschreibung
[hidden]
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0877341
- UMLS CUI [1,2]
- C0543467
Beschreibung
[hidden]
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0013216
- UMLS CUI [1,2]
- C1566537
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C1536080
Beschreibung
[hidden]
Datentyp
date
Alias
- UMLS CUI [1]
- C3260278
Beschreibung
CEC Status
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C1444748
Beschreibung
[hidden]
Datentyp
integer
Alias
- UMLS CUI [1]
- C0449438
Beschreibung
[read-only]
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0443172
Beschreibung
[hidden]
Datentyp
integer
Alias
- UMLS CUI [1]
- C0184806
Beschreibung
[hidden]
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1515023
- UMLS CUI [1,4]
- C0011008
Beschreibung
[hidden]
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1514756
- UMLS CUI [1,4]
- C0011008
Beschreibung
[hidden]
Datentyp
integer
Alias
- UMLS CUI [1]
- C0184806
Beschreibung
[hidden]
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1515023
- UMLS CUI [1,4]
- C0011008
Beschreibung
[hidden]
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1514756
- UMLS CUI [1,4]
- C0011008
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C0947611
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C2826275
Beschreibung
Use SAE Sequence number from the corresponding SAE form (the last item on the form, in the "Non-Clinical" section) [hidden].
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348585
Beschreibung
Copy Serious Adverse Event term from corresponding SAE form [hidden].
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C2826934
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C1515023 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
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