ID
31487
Description
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
Keywords
Versions (1)
- 8/28/18 8/28/18 -
Copyright Holder
GlaxoSmithKline
Uploaded on
August 28, 2018
DOI
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License
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
Description
Blood Transfusion Record
Alias
- UMLS CUI-1
- C0005841
- UMLS CUI-2
- C0034869
Description
Blood Transfusion; Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C0011008
Description
Blood Transfusion; Start Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C1301880
Description
Blood Transfusion; Type
Data type
text
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C0332307
Description
Blood Transfusion, autologous; quantity
Data type
integer
Alias
- UMLS CUI [1,1]
- C0005842
- UMLS CUI [1,2]
- C1265611
Description
Blood Transfusion, homologous; quantity
Data type
integer
Alias
- UMLS CUI [1,1]
- C0005841
- UMLS CUI [1,2]
- C0301883
- UMLS CUI [1,3]
- C1265611
Similar models
Blood Transfusion Record
- StudyEvent: ODM
C0445204 (UMLS CUI-2)
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C0445204 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0445204 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0034869 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
C0301883 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])