ID

32155

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. 22/10/18 22/10/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

22 de octubre 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

Visit 03

1 formularios  
  1. StudyEvent: ODM
    1. Visit 03
Follow-Up Record Day 30 ± 2 or Last Contact Information
Descripción

Follow-Up Record Day 30 ± 2 or Last Contact Information

Alias
UMLS CUI-1
C1522577
Type of contact
Descripción

Follow-up; contact; Type

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C0332158
UMLS CUI [1,3]
C0332307
Contact made by
Descripción

Follow-up; Communication contact

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C1705415
Contact with
Descripción

Follow-up; Communication contact

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C1705415
Discharge
Descripción

Discharge

Alias
UMLS CUI-1
C0030685
Date of discharge
Descripción

Discharge date

Tipo de datos

date

Alias
UMLS CUI [1]
C2361123
Patient still hospitalized at last contact or death during the first hospitalization.
Descripción

Hospitalization; Death in hospital

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019993
UMLS CUI [2]
C0277608
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Similar models

Visit 03

1 formularios
  1. StudyEvent: ODM
    1. Visit 03
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Follow-Up Record Day 30 ± 2 or Last Contact Information
C1522577 (UMLS CUI-1)
Item
Type of contact
text
C1522577 (UMLS CUI [1,1])
C0332158 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
Follow-up; contact; Type
Code List
Type of contact
CL Item
Phone (Phone)
CL Item
Visit (Visit)
CL Item
Letter (Letter)
Item
Contact made by
text
C1522577 (UMLS CUI [1,1])
C1705415 (UMLS CUI [1,2])
Follow-up; contact; Type
Code List
Contact made by
CL Item
Study coordinator/nurse (Study coordinator/nurse)
CL Item
Investigator (Investigator)
CL Item
Other study staff (Other study staff)
Item
Contact with
text
C1522577 (UMLS CUI [1,1])
C1705415 (UMLS CUI [1,2])
Follow-up; contact; Type
Code List
Contact with
CL Item
Patient (Patient)
CL Item
Relative (Relative)
CL Item
Other (Other)
Item Group
Discharge
C0030685 (UMLS CUI-1)
Discharge date
Item
Date of discharge
date
C2361123 (UMLS CUI [1])
Hospitalization; Death in hospital
Item
Patient still hospitalized at last contact or death during the first hospitalization.
boolean
C0019993 (UMLS CUI [1])
C0277608 (UMLS CUI [2])
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