ID

32155

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. 22/10/2018 22/10/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

22 octobre 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

Visit 03

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

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

Alias
UMLS CUI-1
C1522577
Type of contact
Description

Follow-up; contact; Type

Type de données

text

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

Follow-up; Communication contact

Type de données

text

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

Follow-up; Communication contact

Type de données

text

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

Discharge

Alias
UMLS CUI-1
C0030685
Date of discharge
Description

Discharge date

Type de données

date

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

Hospitalization; Death in hospital

Type de données

boolean

Alias
UMLS CUI [1]
C0019993
UMLS CUI [2]
C0277608
Retour au début de la page

Similar models

Visit 03

1 Formulaires
  1. StudyEvent: ODM
    1. Visit 03
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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