ID

31489

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

Unusual Bleeding Form

1 Formulieren  
  1. StudyEvent: ODM
    1. Unusual Bleeding Form
Unusual Bleeding
Beschrijving

Unusual Bleeding

Alias
UMLS CUI-1
C0019080
UMLS CUI-2
C0013227C2700116
Onset date of bleeding
Beschrijving

Hemorrhage; Onset Date

Datatype

date

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0574845
This bleeding corresponds to the following AE form number(s)
Beschrijving

Hemorrhage; AE form number

Datatype

integer

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C1518404
UMLS CUI [1,3]
C0237753
Transfusions
Beschrijving

Hemorrhage; Blood Transfusion

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0005841
Re-operation
Beschrijving

Hemorrhage; repeat surgery

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0035110
Other intervention at surgical site
Beschrijving

Hemorrhage; Operative site, Interventional procedure, Other

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0332850
UMLS CUI [1,3]
C0184661
UMLS CUI [1,4]
C0205394
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Similar models

Unusual Bleeding Form

1 Formulieren
  1. StudyEvent: ODM
    1. Unusual Bleeding Form
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Unusual Bleeding
C0019080 (UMLS CUI-1)
C0013227C2700116 (UMLS CUI-2)
Hemorrhage; Onset Date
Item
Onset date of bleeding
date
C0019080 (UMLS CUI [1,1])
C0574845 (UMLS CUI [1,2])
Hemorrhage; AE form number
Item
This bleeding corresponds to the following AE form number(s)
integer
C0019080 (UMLS CUI [1,1])
C1518404 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
Hemorrhage; Blood Transfusion
Item
Transfusions
boolean
C0019080 (UMLS CUI [1,1])
C0005841 (UMLS CUI [1,2])
Hemorrhage; repeat surgery
Item
Re-operation
boolean
C0019080 (UMLS CUI [1,1])
C0035110 (UMLS CUI [1,2])
Hemorrhage; Operative site, Interventional procedure, Other
Item
Other intervention at surgical site
boolean
C0019080 (UMLS CUI [1,1])
C0332850 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
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