ID

31320

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 (2)
  1. 13/8/18 13/8/18 -
  2. 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

Administrative Data

1 formularios  
  1. StudyEvent: ODM
    1. Administrative Data
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
Investigator Name
Descripción

Investigator; Name

Tipo de datos

text

Alias
UMLS CUI [1]
C2826892
Investigator Name; Address; Telephone; Fax
Descripción

Investigator; Name; Street Address; Telephone; Fax

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2826892
UMLS CUI [1,2]
C1301826
UMLS CUI [1,3]
C1515258
UMLS CUI [1,4]
C1549619
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Similar models

Administrative Data

1 formularios
  1. StudyEvent: ODM
    1. Administrative Data
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])
Investigator; Name
Item
Investigator Name
text
C2826892 (UMLS CUI [1])
Investigator; Name; Street Address; Telephone; Fax
Item
Investigator Name; Address; Telephone; Fax
text
C2826892 (UMLS CUI [1,1])
C1301826 (UMLS CUI [1,2])
C1515258 (UMLS CUI [1,3])
C1549619 (UMLS CUI [1,4])
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