ID
31487
Beschrijving
Study ID: 104619 Clinical Study ID: 63129 Study Title:A multinational, randomized, double-blind comparison of once daily subcutaneous fondaparinux sodium with placebo for the prevention of venous thromboembolic events in acutely ill medical patients (ARTEMIS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fondaparinux sodium Trade Name: Arixtra Study Indication: Thrombosis, Venous
Trefwoorden
Versies (1)
- 2018-08-28 2018-08-28 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
28 augusti 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Subcutaneous fondaparinux sodium for prevention of venous thromboembolic events; Study ID: 104619
Blood Transfusion Record
- StudyEvent: ODM
Beschrijving
Blood Transfusion Record
Alias
- UMLS CUI-1
- C0005841
- UMLS CUI-2
- C0034869
Beschrijving
Blood Transfusion; Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C0011008
Beschrijving
Blood Transfusion; Start Time
Datatype
time
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C1301880
Beschrijving
Blood Transfusion; Type
Datatype
text
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C0332307
Beschrijving
Blood Transfusion, autologous; quantity
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005842
- UMLS CUI [1,2]
- C1265611
Beschrijving
Blood Transfusion, homologous; quantity
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C0301883
- UMLS CUI [1,3]
- C1265611
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