ID
44075
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
Keywords
Versions (2)
- 9/30/18 9/30/18 -
- 9/20/21 9/20/21 -
Copyright Holder
GlaxoSmithKline
Uploaded on
September 20, 2021
DOI
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License
Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; NCT
Hospital Discharge Visit
- StudyEvent: ODM
Description
Hospital Discharge
Alias
- UMLS CUI-1
- C0586514
- UMLS CUI-2
- C0019994
Description
Hospital; Discharge Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0019994
- UMLS CUI [1,2]
- C2361123
Description
Discharge Status
Data type
text
Alias
- UMLS CUI [1]
- C0586514
Description
Final diagnosis (discharge)
Data type
text
Alias
- UMLS CUI [1]
- C0332144
Description
Electrocardiography; C0586514 Discharge status; C1717740 NULL
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1623258
- UMLS CUI [1,2]
- C0586514
- UMLS CUI [1,3]
- C1264639
Description
Electrocardiography; Discharge status; Result
Data type
text
Alias
- UMLS CUI [1,1]
- C1623258
- UMLS CUI [1,2]
- C0586514
- UMLS CUI [1,3]
- C1274040
Description
Hospitalization; Health Resources; Use of
Data type
text
Alias
- UMLS CUI [1,1]
- C0019993
- UMLS CUI [1,2]
- C0018741
- UMLS CUI [1,3]
- C1524063
Description
Clinical events since randomization
Alias
- UMLS CUI-1
- C0877248
Description
Adverse Event; Cessation of life
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0011065
Description
Adverse Event, Myocardial infarction; Adverse Event, Myocardial Reinfarction
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0027051
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C0948369
Description
Adverse Event, Revascularization
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0581603
Description
Adverse Event, Major bleed; Adverse event, Minor bleed
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C3160769
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C3160770
Description
Adverse Event, Cerebrovascular accident
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0038454
Description
Adverse Event, vascular access, Site of access, Hematoma
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750138
- UMLS CUI [1,3]
- C0589360
- UMLS CUI [1,4]
- C0018944
Description
Adverse Event, Pseudoaneurysm
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1510412
Description
Adverse Event, other
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0205394
Description
Interventions since Index PCI
Alias
- UMLS CUI-1
- C0184661
- UMLS CUI-2
- C1711239
- UMLS CUI-3
- C1532338
Description
Interventional Procedure; Coronary Angiography
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0085532
Description
Interventional Procedure; Percutaneous Coronary Intervention; Repeat Surgery
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C1532338
- UMLS CUI [1,3]
- C0035110
Description
Interventional Procedure; Coronary Artery Bypass Surgery
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0010055
Description
Interventional Procedure; Thrombolytic Therapy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0040044
Description
Interventional Procedure; Intra-Aortic Balloon Pumping
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0021860
Description
Interventional Procedure; Vascular Surgical Procedures
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0042381
Description
Concomitant Medication
Alias
- UMLS CUI-1
- C2347852
Description
Unfractionated Heparin [EPC]
Data type
text
Alias
- UMLS CUI [1]
- C2825026
Description
Low Molecular Weight Heparin [EPC]
Data type
text
Alias
- UMLS CUI [1]
- C3536766
Description
Aspirin
Data type
text
Alias
- UMLS CUI [1]
- C0004057
Description
Glycoprotein IIb/IIIa Antagonist
Data type
text
Alias
- UMLS CUI [1]
- C3640054
Description
Bivalirudin; Hirudin
Data type
text
Alias
- UMLS CUI [1]
- C0168273
- UMLS CUI [2]
- C0019573
Description
Clopidogrel
Data type
text
Alias
- UMLS CUI [1]
- C0070166
Description
Ticlopidine
Data type
text
Alias
- UMLS CUI [1]
- C0040207
Description
Oral anticoagulants
Data type
text
Alias
- UMLS CUI [1]
- C0354604
Description
COX II inhibitors
Data type
text
Alias
- UMLS CUI [1]
- C1257954
Description
Anti-Inflammatory Agents, Non-Steroidal; Other
Data type
text
Alias
- UMLS CUI [1,1]
- C0003211
- UMLS CUI [1,2]
- C0205394
Description
Nitrates
Data type
text
Alias
- UMLS CUI [1]
- C0028125
Description
Adrenergic beta-1 Receptor Antagonists
Data type
text
Alias
- UMLS CUI [1]
- C0304516
Description
Calcium Channel Blockers
Data type
text
Alias
- UMLS CUI [1]
- C0006684
Description
Angiotensin-Converting Enzyme Inhibitors
Data type
text
Alias
- UMLS CUI [1]
- C0003015
Description
Angiotensin II receptor antagonist
Data type
text
Alias
- UMLS CUI [1]
- C0521942
Description
Diuretics
Data type
text
Alias
- UMLS CUI [1]
- C0012798
Description
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Data type
text
Alias
- UMLS CUI [1]
- C0360714
Description
Antilipemic agent
Data type
text
Alias
- UMLS CUI [1]
- C0086440
Description
Insulin
Data type
text
Alias
- UMLS CUI [1]
- C0021641
Description
Oral hypoglycemic
Data type
text
Alias
- UMLS CUI [1]
- C0359086
Similar models
Hospital Discharge Visit
- StudyEvent: ODM
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
C2348585 (UMLS CUI [1,2])
C0019994 (UMLS CUI-2)
C2361123 (UMLS CUI [1,2])
C0586514 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0586514 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0018741 (UMLS CUI [1,2])
C1524063 (UMLS CUI [1,3])
C0011065 (UMLS CUI [1,2])
C0027051 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C0948369 (UMLS CUI [2,2])
C0581603 (UMLS CUI [1,2])
C3160769 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C3160770 (UMLS CUI [2,2])
C0038454 (UMLS CUI [1,2])
C0750138 (UMLS CUI [1,2])
C0589360 (UMLS CUI [1,3])
C0018944 (UMLS CUI [1,4])
C1510412 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C1711239 (UMLS CUI-2)
C1532338 (UMLS CUI-3)
C0085532 (UMLS CUI [1,2])
C1532338 (UMLS CUI [1,2])
C0035110 (UMLS CUI [1,3])
C0010055 (UMLS CUI [1,2])
C0040044 (UMLS CUI [1,2])
C0021860 (UMLS CUI [1,2])
C0042381 (UMLS CUI [1,2])
C0019573 (UMLS CUI [2])
C0205394 (UMLS CUI [1,2])