ID

31487

Description

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

Mots-clés

  1. 28/08/2018 28/08/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

28 août 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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Subcutaneous fondaparinux sodium for prevention of venous thromboembolic events; Study ID: 104619

Blood Transfusion Record

Pre-operative Blood Donation
Description

Pre-operative Blood Donation

Alias
UMLS CUI-1
C0005794
UMLS CUI-2
C0445204
Done
Description

Blood Donation; Pre-Operative

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005794
UMLS CUI [1,2]
C0445204
Date
Description

Blood Donation; Pre-Operative; Date in time

Type de données

date

Alias
UMLS CUI [1,1]
C0005794
UMLS CUI [1,2]
C0445204
UMLS CUI [1,3]
C0011008
Total Units
Description

Blood Donation; Pre-Operative; quantity

Type de données

integer

Alias
UMLS CUI [1,1]
C0005794
UMLS CUI [1,2]
C0445204
UMLS CUI [1,3]
C1265611
Blood Transfusion Record
Description

Blood Transfusion Record

Alias
UMLS CUI-1
C0005841
UMLS CUI-2
C0034869
Date Given
Description

Blood Transfusion; Date

Type de données

date

Alias
UMLS CUI [1,1]
C0005841
UMLS CUI [1,2]
C0011008
Start Time
Description

Blood Transfusion; Start Time

Type de données

time

Alias
UMLS CUI [1,1]
C0005841
UMLS CUI [1,2]
C1301880
Transfusion Type
Description

Blood Transfusion; Type

Type de données

text

Alias
UMLS CUI [1,1]
C0005841
UMLS CUI [1,2]
C0332307
Transfused (Units) - Autologous
Description

Blood Transfusion, autologous; quantity

Type de données

integer

Alias
UMLS CUI [1,1]
C0005842
UMLS CUI [1,2]
C1265611
Transfused (Units) - Homologous
Description

Blood Transfusion, homologous; quantity

Type de données

integer

Alias
UMLS CUI [1,1]
C0005841
UMLS CUI [1,2]
C0301883
UMLS CUI [1,3]
C1265611

Similar models

Blood Transfusion Record

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Pre-operative Blood Donation
C0005794 (UMLS CUI-1)
C0445204 (UMLS CUI-2)
Blood Donation; Pre-Operative
Item
Done
boolean
C0005794 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
Blood Donation; Pre-Operative; Date in time
Item
Date
date
C0005794 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Blood Donation; Pre-Operative; quantity
Item
Total Units
integer
C0005794 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Item Group
Blood Transfusion Record
C0005841 (UMLS CUI-1)
C0034869 (UMLS CUI-2)
Blood Transfusion; Date
Item
Date Given
date
C0005841 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Blood Transfusion; Start Time
Item
Start Time
time
C0005841 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Item
Transfusion Type
text
C0005841 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Transfusion Type
CL Item
Whole blood (Whole blood)
CL Item
PRBCís (PRBCís)
CL Item
Reinfusion shed blood (Reinfusion shed blood)
Item
Transfused (Units) - Autologous
integer
C0005842 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Code List
Transfused (Units) - Autologous
Blood Transfusion, homologous; quantity
Item
Transfused (Units) - Homologous
integer
C0005841 (UMLS CUI [1,1])
C0301883 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])

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