ID

31314

Beschrijving

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

Trefwoorden

Versies (2)
  1. 13-08-18 13-08-18 -
  2. 13-08-18 13-08-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

13 augustus 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; Study ID: 104574

Engels

Administrative Data

1 Formulieren  
  1. StudyEvent: ODM
    1. Administrative Data
Administrative Data
Beschrijving

Administrative Data

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

Patient ID; Centre Number

Datatype

text

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

Patient ID; Envelope Number

Datatype

text

Alias
UMLS CUI [1,1]
C1269815
UMLS CUI [1,2]
C2348585
Investigator Name
Beschrijving

Investigator; Name

Datatype

text

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

Investigator; Name; Street Address; Telephone; Fax

Datatype

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 Formulieren
  1. StudyEvent: ODM
    1. Administrative Data
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

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