ID

31484

Beschrijving

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

Trefwoorden

Versies (1)
  1. 28-08-18 28-08-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

28 augustus 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Subcutaneous fondaparinux sodium for prevention of venous thromboembolic events; Study ID: 104619

Engels

Autopsy Form

1 Formulieren  
  1. StudyEvent: ODM
    1. Autopsy Form
Autopsy
Beschrijving

Autopsy

Alias
UMLS CUI-1
C0004398
Was an autopsy performed?
Beschrijving

Autopsy

Datatype

boolean

Alias
UMLS CUI [1]
C0004398
Date of autopsy
Beschrijving

Autopsy; Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0004398
UMLS CUI [1,2]
C0011008
Pulmonary Embolism
Beschrijving

Pulmonary Embolism

Datatype

text

Alias
UMLS CUI [1]
C0034065
Deep Vein Thrombosis
Beschrijving

Deep Vein Thrombosis

Datatype

text

Alias
UMLS CUI [1]
C0149871
Other thrombosis
Beschrijving

Thrombosis; Other

Datatype

text

Alias
UMLS CUI [1,1]
C0040053
UMLS CUI [1,2]
C0205394
Hemorrhage
Beschrijving

Hemorrhage

Datatype

text

Alias
UMLS CUI [1]
C0019080
Other findings
Beschrijving

Other findings

Datatype

text

Alias
UMLS CUI [1]
C0159135
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Similar models

Autopsy Form

1 Formulieren
  1. StudyEvent: ODM
    1. Autopsy Form
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Autopsy
C0004398 (UMLS CUI-1)
Autopsy
Item
Was an autopsy performed?
boolean
C0004398 (UMLS CUI [1])
Autopsy; Date in time
Item
Date of autopsy
date
C0004398 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Pulmonary Embolism
text
C0034065 (UMLS CUI [1])
Pulmonary Embolism
Code List
Pulmonary Embolism
CL Item
No (No)
CL Item
Yes - Left pulmonary artery (Yes - Left pulmonary artery)
CL Item
Yes - Left lobar arteries (Yes - Left lobar arteries)
CL Item
Yes - Left segmental arteries (Yes - Left segmental arteries)
CL Item
Yes - Main pulmonary trunk (Yes - Main pulmonary trunk)
CL Item
Yes - Right pulmonary artery (Yes - Right pulmonary artery)
CL Item
Yes - Right lobar arteries (Yes - Right lobar arteries)
CL Item
Yes - Right segmental arteries (Yes - Right segmental arteries)
Item
Deep Vein Thrombosis
text
C0149871 (UMLS CUI [1])
Deep Vein Thrombosis
Code List
Deep Vein Thrombosis
CL Item
No (No)
CL Item
Yes - Left calf vein (Yes - Left calf vein)
CL Item
Yes - Left popliteal vein (Yes - Left popliteal vein)
CL Item
Yes - Left femoral vein (Yes - Left femoral vein)
CL Item
Yes - Left iliac vein (Yes - Left iliac vein)
CL Item
Yes - Inferior vena cava (Yes - Inferior vena cava)
CL Item
Yes - Right calf vein (Yes - Right calf vein)
CL Item
Yes - Right popliteal vein (Yes - Right popliteal vein)
CL Item
Yes - Right femoral vein (Yes - Right femoral vein)
CL Item
Yes - Right iliac vein (Yes - Right iliac vein)
Item
Other thrombosis
text
C0040053 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Thrombosis; Other
Code List
Other thrombosis
CL Item
No (No)
CL Item
Yes (specify) (Yes (specify))
Item
Hemorrhage
text
C0019080 (UMLS CUI [1])
Thrombosis; Other
Code List
Hemorrhage
CL Item
No (No)
CL Item
Yes (specify) (Yes (specify))
Item
Other findings
text
C0159135 (UMLS CUI [1])
Other findings
Code List
Other findings
CL Item
No (No)
CL Item
Yes (specify) (Yes (specify))
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