ID
37192
Beschreibung
Aspirin Responsiveness and Outcome in Coronary Artery Bypass Graft (CABG) Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT01174862 In patients undergoing coronary artery bypass graft (CAGB) surgery, aspirin is commonly prescribed to prevent graft thrombosis and myocardial ischemia. However, there are still a significant number of grafts occluding in the postoperative period. This is partly attributed to reduced aspirin responsiveness, also called "aspirin resistance". At the moment, no standardized definition or laboratory test is available to quantify "aspirin resistance", and strong platelet reactivity in laboratory tests is not necessarily associated with increased thrombotic events. However, there is increasing evidence that reduced aspirin responsiveness in platelet function analyzers is associated with adverse long-term outcome and higher incidence of major adverse events in patients with stable coronary artery disease and in patients undergoing percutaneous coronary intervention. In patients undergoing coronary artery bypass graft surgery, the predictive value of a laboratory finding of reduced aspirin responsiveness remains unclear. Therefore, the aim of this study is to prospectively evaluate whether the pre- and/or postoperative laboratory finding of reduced aspirin responsiveness defined by MultiplateTM platelet function analyzer is associated with higher incidences of adverse outcome after 30 days and 12 months in patients undergoing CABG surgery.
Link
https://clinicaltrials.gov/show/NCT01174862
Stichworte
Versionen (1)
- 07.07.19 07.07.19 -
Rechteinhaber
University Hospital, Basel, Switzerland
Hochgeladen am
7. Juli 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Aspirin Responsiveness and Coronary Artery Bypass Graft NCT01174862
Eligibility Criteria
- StudyEvent: Eligibility
Beschreibung
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschreibung
Missing written consent
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1705492
- UMLS CUI [1,2]
- C0009797
Beschreibung
Aspirin therapy insufficient
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1705492
- UMLS CUI [1,2]
- C4303556
- UMLS CUI [2,1]
- C4303556
- UMLS CUI [2,2]
- C0419823
- UMLS CUI [2,3]
- C0445204
- UMLS CUI [2,4]
- C4018905
Beschreibung
Clopidogrel treatment
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0070166
- UMLS CUI [1,2]
- C3810854
- UMLS CUI [1,3]
- C4255413
Beschreibung
Emergency surgery
Datentyp
boolean
Alias
- UMLS CUI [1]
- C4264510
Beschreibung
More than CABG
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0439093
- UMLS CUI [1,3]
- C0010055
Beschreibung
Platelet disorders
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1744681
- UMLS CUI [1,2]
- C0005818
- UMLS CUI [2]
- C0398636
Beschreibung
SSRI therapy
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0360105
Beschreibung
Severe Hepatopathy
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0023895
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [2]
- C0086890
Beschreibung
Severe kidney disease
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0205082
- UMLS CUI [1,2]
- C0022658
Ähnliche Modelle
Eligibility Criteria
- StudyEvent: Eligibility
C0010055 (UMLS CUI [1,2])
C3810854 (UMLS CUI [1,2])
C4255413 (UMLS CUI [1,3])
C0009797 (UMLS CUI [1,2])
C4303556 (UMLS CUI [1,2])
C4303556 (UMLS CUI [2,1])
C0419823 (UMLS CUI [2,2])
C0445204 (UMLS CUI [2,3])
C4018905 (UMLS CUI [2,4])
C3810854 (UMLS CUI [1,2])
C4255413 (UMLS CUI [1,3])
C0439093 (UMLS CUI [1,2])
C0010055 (UMLS CUI [1,3])
C0005818 (UMLS CUI [1,2])
C0398636 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C0086890 (UMLS CUI [2])
C0022658 (UMLS CUI [1,2])