ID
31317
Beschreibung
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 USE THIS PAGE ONLY FOR THOSE PATIENTS WHO DID NOT COMPLETE 30 DAY FOLLOW-UP VISIT (as per protocol, that is, 30-35 days from randomization)
Stichworte
Versionen (2)
- 13/8/18 13/8/18 -
- 13/8/18 13/8/18 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
13 de agosto de 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; NCT
Contact Form
- StudyEvent: ODM
Beschreibung
Contact
Alias
- UMLS CUI-1
- C0332158
- UMLS CUI-2
- C0681850
Beschreibung
Successful contact made
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0332158
- UMLS CUI [1,2]
- C0681850
- UMLS CUI [1,3]
- C0597535
Beschreibung
Successful contact made; date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0332158
- UMLS CUI [1,2]
- C0681850
- UMLS CUI [1,3]
- C0011008
Beschreibung
date form completed
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0332158
- UMLS CUI [1,2]
- C0681850
- UMLS CUI [1,3]
- C1115437
Beschreibung
Contact made by
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0337611
- UMLS CUI [1,2]
- C1272683
Beschreibung
Follow-up; method
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1522577
- UMLS CUI [1,2]
- C0025663
Beschreibung
contact person
Datentyp
text
Alias
- UMLS CUI [1]
- C0337611
Beschreibung
Death
Datentyp
text
Alias
- UMLS CUI [1]
- C0011065
Beschreibung
myocardal infarction; myocardial reinfarction
Datentyp
text
Alias
- UMLS CUI [1]
- C0027051
- UMLS CUI [2]
- C0948369
Beschreibung
Cerebrovascular event
Datentyp
text
Alias
- UMLS CUI [1]
- C0038454
Beschreibung
PCI; stent
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C0038257
Beschreibung
CABG
Datentyp
text
Alias
- UMLS CUI [1]
- C0010055
Beschreibung
Bleeding
Datentyp
text
Alias
- UMLS CUI [1]
- C0019080
Beschreibung
Comments
Datentyp
text
Alias
- UMLS CUI [1]
- C0947611
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- StudyEvent: ODM
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C0597535 (UMLS CUI [1,3])
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C0038257 (UMLS CUI [1,2])