ID

31486

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

Versions (1)
  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

Anglais

Medication Record

1 Formulaires  
  1. StudyEvent: ODM
    1. Medication Record
Meditation Record
Description

Meditation Record

Alias
UMLS CUI-1
C2734539
Drug Name
Description

Medication Name

Type de données

text

Alias
UMLS CUI [1]
C2360065
Total Daily Dose/Units
Description

Medication Dose; Daily Dose

Type de données

float

Alias
UMLS CUI [1,1]
C3174092
UMLS CUI [1,2]
C2348070
Route
Description

Drug Administration Routes

Type de données

text

Alias
UMLS CUI [1]
C0013153
Prior or after?
Description

Drug Administration; Time

Type de données

text

Alias
UMLS CUI [1,1]
C3469597
UMLS CUI [1,2]
C0040223
Duration Dates - Start Date
Description

Pharmaceutical Preparations; Start Date

Type de données

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
Duration Dates - End Date
Description

Pharmaceutical Preparations; End Date

Type de données

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Indication
Description

Pharmaceutical Preparations; Indication

Type de données

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C3146298
A.E. Form Number
Description

Pharmaceutical Preparations; Adverse Event Document Number

Type de données

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0877248
UMLS CUI [1,3]
C1704732
UMLS CUI [1,4]
C0237753
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Similar models

Medication Record

1 Formulaires
  1. StudyEvent: ODM
    1. Medication Record
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Meditation Record
C2734539 (UMLS CUI-1)
Medication Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
Medication Dose; Daily Dose
Item
Total Daily Dose/Units
float
C3174092 (UMLS CUI [1,1])
C2348070 (UMLS CUI [1,2])
Drug Administration Routes
Item
Route
text
C0013153 (UMLS CUI [1])
Item
Prior or after?
text
C3469597 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Drug Administration; Time
Code List
Prior or after?
CL Item
Prior (Prior)
CL Item
After (After)
Pharmaceutical Preparations; Start Date
Item
Duration Dates - Start Date
date
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Pharmaceutical Preparations; End Date
Item
Duration Dates - End Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Pharmaceutical Preparations; Indication
Item
Indication
text
C0013227 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
Pharmaceutical Preparations; Adverse Event Document Number
Item
A.E. Form Number
integer
C0013227 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
C1704732 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
Retour au début de la page 

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