ID

31326

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 (1)
  1. 8/13/18 8/13/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 13, 2018

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; Clinical Study ID: AR1104574

English

Death Report

1 forms  
  1. StudyEvent: ODM
    1. Death Report
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Patient ID, Centre No.
Description

Patient ID; Centre Number

Data type

text

Alias
UMLS CUI [1,1]
C1269815
UMLS CUI [1,2]
C2825181
UMLS CUI [1,3]
C1300638
Patient ID, Envelope No.
Description

Patient ID; Envelope Number

Data type

text

Alias
UMLS CUI [1,1]
C1269815
UMLS CUI [1,2]
C2348585
Patient Initials
Description

Patient Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Date of Death
Description

Date of Death

Data type

date

Alias
UMLS CUI [1]
C1148348
Time of Death
Description

Time of Death

Data type

time

Alias
UMLS CUI [1]
C1301931
Cause of Death
Description

Cause of Death

Alias
UMLS CUI-1
C0007465
Cardiac
Description

Cause of Death, cardiac

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0018799
Other Vascular
Description

Cause of Death; Vascular

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0042373
Cause of Death unknown
Description

Cause of Death unknown

Data type

boolean

Alias
UMLS CUI [1]
C0277589
Non-Cardiovascular
Description

Cause of death; non-cardiovascular

Data type

boolean

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C1298908
UMLS CUI [1,3]
C0007222
30-Day Follow-Up Visit completed
Description

Follow-Up Visit complete

Data type

boolean

Alias
UMLS CUI [1,1]
C0589121
UMLS CUI [1,2]
C0205197
Study completion completed
Description

Study completion complete

Data type

boolean

Alias
UMLS CUI [1,1]
C2826674
UMLS CUI [1,2]
C0205197
Was an autopsy performed?
Description

autopsy

Data type

boolean

Alias
UMLS CUI [1]
C0004398
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Similar models

Death Report

1 forms
  1. StudyEvent: ODM
    1. Death Report
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Patient ID; Centre Number
Item
Patient ID, Centre No.
text
C1269815 (UMLS CUI [1,1])
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
Patient ID; Envelope Number
Item
Patient ID, Envelope No.
text
C1269815 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Date of Death
Item
Date of Death
date
C1148348 (UMLS CUI [1])
Time of Death
Item
Time of Death
time
C1301931 (UMLS CUI [1])
Item Group
Cause of Death
C0007465 (UMLS CUI-1)
Item
Cardiac
text
C0007465 (UMLS CUI [1,1])
C0018799 (UMLS CUI [1,2])
Cause of Death, cardiac
Code List
Cardiac
CL Item
Reinfarction/New infarction (Reinfarction/New infarction)
CL Item
Asystole (Asystole)
CL Item
Ventricular Fibrillation (Ventricular Fibrillation)
CL Item
Electromechanical Dissociation (Electromechanical Dissociation)
CL Item
Other Sudden or Arrhythmic Death (Other Sudden or Arrhythmic Death)
CL Item
Congestive Heart Failure (Congestive Heart Failure)
CL Item
Cardiogenic Shock (Cardiogenic Shock)
CL Item
Ventricular Septal Defect (Ventricular Septal Defect)
CL Item
Myocardial Free Wall Rupture (Myocardial Free Wall Rupture)
CL Item
Cardiac Tamponade (Cardiac Tamponade)
CL Item
Other (Other)
Item
Other Vascular
text
C0007465 (UMLS CUI [1,1])
C0042373 (UMLS CUI [1,2])
Cause of Death; Vascular
Code List
Other Vascular
CL Item
Stroke (Stroke)
CL Item
Peripheral Vascular Disease (Peripheral Vascular Disease)
CL Item
Aortic Dissection/Rupture (Aortic Dissection/Rupture)
CL Item
Pulmonary Embolus (Pulmonary Embolus)
CL Item
Hemorrhage (Hemorrhage)
CL Item
Other (Other)
Cause of Death unknown
Item
boolean
C0277589 (UMLS CUI [1])
Cause of death; non-cardiovascular
Item
Non-Cardiovascular
boolean
C0007465 (UMLS CUI [1,1])
C1298908 (UMLS CUI [1,2])
C0007222 (UMLS CUI [1,3])
Follow-Up Visit complete
Item
30-Day Follow-Up Visit completed
boolean
C0589121 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Study completion complete
Item
Study completion completed
boolean
C2826674 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
autopsy
Item
Was an autopsy performed?
boolean
C0004398 (UMLS CUI [1])
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