ID

31316

Descripción

Study ID: 104574 Clinical Study ID: AR1104574 Study Title: A randomized blinded pilot trial of fondaparinux sodium (Arixtra®) versus unfractionated heparin in addition to standard therapy in a broad range of patients undergoing percutaneous coronary intervention (ASPIRE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: fondaparinux sodium Trade Name: Arixtra Study Indication: Thromboembolism

Palabras clave

Versiones (1)
  1. 13/8/18 13/8/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

13 de agosto de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; Clinical Study ID: AR1104574

Inglés

Study Completion/Investigator's Final Statement

1 formularios  
Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Patient ID, Centre No.
Descripción

Patient ID; Centre Number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1269815
UMLS CUI [1,2]
C2825181
UMLS CUI [1,3]
C1300638
Patient ID, Envelope No.
Descripción

Patient ID; Envelope Number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1269815
UMLS CUI [1,2]
C2348585
Patient Initials
Descripción

Patient Initials

Tipo de datos

text

Alias
UMLS CUI [1]
C2986440
Final statement
Descripción

Final statement

Alias
UMLS CUI-1
C0008961
UMLS CUI-2
C1710187
Was the study drug unblinded at any time during the study?
Descripción

study drug unblinded

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C3897431
Did patient withdraw consent during the study?
Descripción

consent withdrawn

Tipo de datos

text

Alias
UMLS CUI [1]
C1707492
Additional comments
Descripción

Comment

Tipo de datos

text

Alias
UMLS CUI [1]
C0947611
Investigator's signature
Descripción

Investigator's signature

Tipo de datos

text

Alias
UMLS CUI [1]
C2346576
Please print investigator last name in block capitals
Descripción

investigator last name

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C1301584
Date of signature
Descripción

Investigator signature, date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
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Similar models

Study Completion/Investigator's Final Statement

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Patient ID; Centre Number
Item
Patient ID, Centre No.
text
C1269815 (UMLS CUI [1,1])
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
Patient ID; Envelope Number
Item
Patient ID, Envelope No.
text
C1269815 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Item Group
Final statement
C0008961 (UMLS CUI-1)
C1710187 (UMLS CUI-2)
Item
Was the study drug unblinded at any time during the study?
text
C0304229 (UMLS CUI [1,1])
C3897431 (UMLS CUI [1,2])
study drug unblinded
Code List
Was the study drug unblinded at any time during the study?
CL Item
No (No)
CL Item
Yes (Specify) (Yes (Specify))
Item
Did patient withdraw consent during the study?
text
C1707492 (UMLS CUI [1])
consent withdrawn
Code List
Did patient withdraw consent during the study?
CL Item
No (No)
CL Item
Yes (give date) (Yes (give date))
Comment
Item
Additional comments
text
C0947611 (UMLS CUI [1])
Investigator's signature
Item
Investigator's signature
text
C2346576 (UMLS CUI [1])
investigator last name
Item
Please print investigator last name in block capitals
text
C0008961 (UMLS CUI [1,1])
C1301584 (UMLS CUI [1,2])
Investigator signature, date
Item
Date of signature
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Volver a la parte superior de la página 

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