ID
31324
Beskrivning
Study ID: 104574 Clinical Study ID: AR1104574 Study Title: A randomized blinded pilot trial of fondaparinux sodium (Arixtra®) versus unfractionated heparin in addition to standard therapy in a broad range of patients undergoing percutaneous coronary intervention (ASPIRE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: fondaparinux sodium Trade Name: Arixtra Study Indication: Thromboembolism
Nyckelord
Versioner (1)
- 2018-08-13 2018-08-13 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
13 augusti 2018
DOI
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Licens
Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; Clinical Study ID: AR1104574
Adverse Event Report
- StudyEvent: ODM
Beskrivning
Adverse event
Alias
- UMLS CUI-1
- C0877248
Beskrivning
Adverse event
Datatyp
text
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
Adverse event; Date of onset
Datatyp
date
Alias
- UMLS CUI [1]
- C2985916
Beskrivning
Adverse event; start time
Datatyp
time
Alias
- UMLS CUI [1]
- C2697889
Beskrivning
Adverse event; maximum intensity
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0518690
Beskrivning
Adverse event; Relationship; study drug
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0013230
Beskrivning
Adverse event; Relationship; study drug; action taken
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0013230
- UMLS CUI [1,4]
- C2826626
Beskrivning
Adverse event; Relationship; study drug; corrective therapies
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0013230
- UMLS CUI [1,4]
- C0087111
- UMLS CUI [1,5]
- C0719519
Beskrivning
Adverse event; Outcome
Datatyp
text
Alias
- UMLS CUI [1]
- C1705586
Beskrivning
Adverse event; seriousness criteria
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1710056
Beskrivning
Adverse event; seriousness; date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0808070
Beskrivning
Adverse event; seriousness; time
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C1301880
Beskrivning
Adverse event; seriousness criteria
Datatyp
text
Alias
- UMLS CUI [1]
- C1710056
Beskrivning
Adverse event; significan bleeding
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C0019080
Similar models
Adverse Event Report
- StudyEvent: ODM
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
C2348585 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
C0439849 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
C2826626 (UMLS CUI [1,4])
C0439849 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
C0087111 (UMLS CUI [1,4])
C0719519 (UMLS CUI [1,5])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C0019080 (UMLS CUI [1,2])