ID
31325
Descripción
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
Palabras clave
Versiones (1)
- 13/8/18 13/8/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
13 de agosto de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; Clinical Study ID: AR1104574
SAE Complementary Report
- StudyEvent: ODM
Descripción
Serious advert event
Alias
- UMLS CUI-1
- C1519255
Descripción
Serious advert event; date of onset
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0574845
Descripción
Serious advert event; time of onset
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1301880
Descripción
Serious advert event; description
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0678257
Descripción
Serious advert event; concomitant medications
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
Descripción
Medical History; Serious advert events
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C1519255
Descripción
Concomitant diseases; Serious advert events
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1519255
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SAE Complementary Report
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C1301880 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])