ID

31486

Descripción

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

Palabras clave

Versiones (1)
  1. 28/8/18 28/8/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

28 de agosto de 2018

DOI

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Licencia

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

Inglés

Medication Record

1 formularios  
  1. StudyEvent: ODM
    1. Medication Record
Meditation Record
Descripción

Meditation Record

Alias
UMLS CUI-1
C2734539
Drug Name
Descripción

Medication Name

Tipo de datos

text

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

Medication Dose; Daily Dose

Tipo de datos

float

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

Drug Administration Routes

Tipo de datos

text

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

Drug Administration; Time

Tipo de datos

text

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

Pharmaceutical Preparations; Start Date

Tipo de datos

date

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

Pharmaceutical Preparations; End Date

Tipo de datos

date

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

Pharmaceutical Preparations; Indication

Tipo de datos

text

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

Pharmaceutical Preparations; Adverse Event Document Number

Tipo de datos

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 formularios
  1. StudyEvent: ODM
    1. Medication Record
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
Volver a la parte superior de la página 

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