ID

31488

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

Keywords

Versions (1)
  1. 8/28/18 8/28/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 28, 2018

DOI

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License

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

English

End of Treatment/End of Study

1 forms  
End of Treatment
Description

End of Treatment

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C0444930
Date of last administration
Description

Pharmaceutical Preparations; Date last dose

Data type

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1762893
Main reason for stopping treatment (tick one box only)
Description

Pharmaceutical preparations, end; Reason

Data type

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0444930
UMLS CUI [1,3]
C0566251
End of Study
Description

End of Study

Alias
UMLS CUI-1
C0008972
UMLS CUI-2
C0444930
Date of end of study
Description

Study end Date

Data type

date

Alias
UMLS CUI [1]
C2983670
Main reason for stopping study (tick one box only)
Description

Clinical Research, end; Reason

Data type

text

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C0444930
UMLS CUI [1,3]
C0566251
Was the study code broken at any time?
Description

Clinical Research; study code

Data type

boolean

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C0805701
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Similar models

End of Treatment/End of Study

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
End of Treatment
C0087111 (UMLS CUI-1)
C0444930 (UMLS CUI-2)
Pharmaceutical Preparations; Date last dose
Item
Date of last administration
date
C0013227 (UMLS CUI [1,1])
C1762893 (UMLS CUI [1,2])
Item
Main reason for stopping treatment (tick one box only)
text
C0013227 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Therapeutic Procedure; End; Reason
Code List
Main reason for stopping treatment (tick one box only)
CL Item
Lack of efficacy (Lack of efficacy)
CL Item
Adverse event (Adverse event)
CL Item
Subject's request (Subject's request)
CL Item
Subject lost to follow-up (Subject lost to follow-up)
CL Item
Other reason (specify) (Other reason (specify))
CL Item
Poor compliance to protocol (Poor compliance to protocol)
CL Item
Completed study treatment period (Completed study treatment period)
Item Group
End of Study
C0008972 (UMLS CUI-1)
C0444930 (UMLS CUI-2)
Study end Date
Item
Date of end of study
date
C2983670 (UMLS CUI [1])
Item
Main reason for stopping study (tick one box only)
text
C0008972 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Therapeutic Procedure; End; Reason
Code List
Main reason for stopping study (tick one box only)
CL Item
Lack of efficacy (Lack of efficacy)
CL Item
Adverse event (Adverse event)
CL Item
Subject's request (Subject's request)
CL Item
Subject lost to follow-up (Subject lost to follow-up)
CL Item
Other reason (specify) (Other reason (specify))
CL Item
Completed follow-up period (Completed follow-up period)
Clinical Research; study code
Item
Was the study code broken at any time?
boolean
C0008972 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
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