ID
31321
Description
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 USE THIS PAGE ONLY FOR THOSE PATIENTS WHO DID NOT COMPLETE 30 DAY FOLLOW-UP VISIT (as per protocol, that is, 30-35 days from randomization)
Mots-clés
Versions (2)
- 13/08/2018 13/08/2018 -
- 13/08/2018 13/08/2018 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
13 août 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Fondaparinux sodium (Arixtra) versus unfractionated heparin with patients undergoing PCI; Clinical Study ID: AR1104574
Contact Form
- StudyEvent: ODM
Description
Contact
Alias
- UMLS CUI-1
- C0332158
- UMLS CUI-2
- C0681850
Description
Successful contact made
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0332158
- UMLS CUI [1,2]
- C0681850
- UMLS CUI [1,3]
- C0597535
Description
Successful contact made; date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0332158
- UMLS CUI [1,2]
- C0681850
- UMLS CUI [1,3]
- C0011008
Description
date form completed
Type de données
date
Alias
- UMLS CUI [1,1]
- C0332158
- UMLS CUI [1,2]
- C0681850
- UMLS CUI [1,3]
- C1115437
Description
Contact made by
Type de données
text
Alias
- UMLS CUI [1,1]
- C0337611
- UMLS CUI [1,2]
- C1272683
Description
Follow-up; method
Type de données
text
Alias
- UMLS CUI [1,1]
- C1522577
- UMLS CUI [1,2]
- C0025663
Description
contact person
Type de données
text
Alias
- UMLS CUI [1]
- C0337611
Description
Death
Type de données
text
Alias
- UMLS CUI [1]
- C0011065
Description
myocardal infarction; myocardial reinfarction
Type de données
text
Alias
- UMLS CUI [1]
- C0027051
- UMLS CUI [2]
- C0948369
Description
Cerebrovascular event
Type de données
text
Alias
- UMLS CUI [1]
- C0038454
Description
PCI; stent
Type de données
text
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C0038257
Description
CABG
Type de données
text
Alias
- UMLS CUI [1]
- C0010055
Description
Bleeding
Type de données
text
Alias
- UMLS CUI [1]
- C0019080
Description
Comments
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Similar models
Contact Form
- StudyEvent: ODM
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
C2348585 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,2])
C0597535 (UMLS CUI [1,3])
C0681850 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0681850 (UMLS CUI [1,2])
C1115437 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,2])
C0025663 (UMLS CUI [1,2])
C0948369 (UMLS CUI [2])
C0038257 (UMLS CUI [1,2])