ID
31323
Description
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
Mots-clés
Versions (1)
- 13/08/2018 13/08/2018 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
13 août 2018
DOI
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Licence
Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; Clinical Study ID: AR1104574
Stroke Report
- StudyEvent: ODM
Description
Stroke
Alias
- UMLS CUI-1
- C0038454
Description
Cerebrovascular event; onset date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0574845
Description
Cerebrovascular event; time of onset
Type de données
time
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0449244
Description
Cerebrovascular event; Hospitalization
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0019993
Description
Cerebrovascular event; Hospitalization
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0019993
Description
Cerebrovascular event; Symptoms
Type de données
text
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C1457887
Description
Cerebrovascular event; status
Type de données
text
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0018759
Description
Cerebrovascular event; effect
Type de données
text
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C1879646
Description
Cerebrovascualr event; antithrombotic medications
Type de données
text
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C1704311
Description
Cerebrovascular event; invasive procedure
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C1548804
Description
Cerebrovascular event; Diagnostic Tests
Type de données
text
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0086143
Description
Cerebrovascular event; Final Diagnosis
Type de données
text
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C1546485
Similar models
Stroke Report
- StudyEvent: ODM
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
C2348585 (UMLS CUI [1,2])
C0574845 (UMLS CUI [1,2])
C0449244 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,2])
C1879646 (UMLS CUI [1,2])
C1704311 (UMLS CUI [1,2])
C1548804 (UMLS CUI [1,2])
C0086143 (UMLS CUI [1,2])
C1546485 (UMLS CUI [1,2])