Coronary Artery Bypass Grafting: Factors Related to Late Events and Saphenous Graft Patency

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2008 by Centro Cardiologico Monzino.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Centro Cardiologico Monzino
ClinicalTrials.gov Identifier:
NCT00755248
First received: September 16, 2008
Last updated: NA
Last verified: September 2008
History: No changes posted

September 16, 2008
September 16, 2008
January 2007
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Not Provided
Not Provided
No Changes Posted
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Coronary Artery Bypass Grafting: Factors Related to Late Events and Saphenous Graft Patency
Coronary Artery Bypass Grafting: Factors Related to Late Events and Saphenous Graft Patency

The purpose of this study is to determine the relations between conventional and unconventional risk factors and adverse clinical events at follow-up (including coronary bypass patency) in patients undergoing surgical myocardial revascularization.

Coronary artery bypass grafting represents one of the most frequent surgical procedure performed in the United States and Europe. The clinical benefit of myocardial revascularization is related to freedom of adverse cardiovascular events and to graft patency, above all of great saphenous vein, which is nowadays the main autologous vessel used for grafting coronaries different from anterior interventricular artery. Unfortunately, phenomena leading to early and, above all, late complications and to graft occlusion are not fully clarified and it so not possible to explain interindividual and temporary variability of progressive stenosis rate only on the basis of classical atherosclerosis risk factors. The aim of our study is to prospectively study the role of conventional risk factors (preoperative risk factors and clinical features) and of unconventional risk factors (genetic polymorphisms, inflammation and coagulation markers) with saphenous late patency and postoperative patients outcome, in particular with regard to adverse clinical events (myocardial infarction, successive stenting procedures, arrhythmias etc.)and to bypass patency.

Plasma venous samples will be collected the day before surgery, at discharge from the hospital, and at follow-up from patients undergoing on-pump and off-pump coronary artery bypass grafting and stored at -80°C; Patients will be followed-up periodically with visits and telephone interviews, and will be also invited to undergo multislice (64 rows) CT scan in order to assess graft patency between 12 and 24 months after surgery.

Finally the relation between conventional and unconventional risk factors with adverse events at follow-up will be assessed with multivariable statistical models.

Observational
Observational Model: Case-Only
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
Description:

Plasma,serum, whole blood

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  • Myocardial Revascularization
  • Atherosclerosis
Procedure: Coronary Artery Bypass Grafting
Coronary Artery Bypass Grafting on- or off-pump
1
Pts undergoing CABG or OPCAB
Intervention: Procedure: Coronary Artery Bypass Grafting
1. American Heart Association. Heart disease and stroke statistics - 2005 update. Dallas, TX: AHA 2004 2. Lytle BW. Prolonging patency - choosing coronary bypass grafts. N Engl J Med 2004; 351: 2262-4 3. Motwani JG et al. Aortocoronary saphenous vein graft disease : pathogenesis, predisposition and prevention. Circulation 1998; 97:916-31 4. Yilmaz M et al. Metabolic syndrome negatively impacts early patency of saphenous vein grafts. Coronary artery disease 2006; 17:41-4 5. Moor E et al. Haemostatic function in patients undergoing coronary artery bypass grafting: perioperative perturbations and relations to saphenous vein graft closure. Thrombosis research 2000; 98:39-49 6. Podgoreanu M et al. New paradigms in cardiovascular medicine. JACC 2005; 46:1965-77 7. Stafford-Smith M et al. Association of genetic polymorphisms with risk of renal injury after coronary bypass graft surgery. Am J Kidney Dusease 2005; 45:519-30 8. Moor E et al. Coagulation factor V (Arg506à Gln) mutation and early saphenous graft occlusion after coronary artery bypass grafting. Thromb Haemost 1998; 80:220-4 9. Yende S et al. Clinical relevance of ACE gene polymorphisms topredict risk of mechanical ventilation after coronary artery bypass surgery. Crit Care Med 2004; 32: 922-27

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
300
January 2011
Not Provided

Inclusion Criteria:

  • Men and women age 18 to 89
  • Elective primary CABG
  • Female patients must be non-lactating and not pregnant
  • Able and willing to comply with study requirements by signing a consent form

Exclusion criteria

  • Concomitant surgery
  • Major end organ dysfunction
  • Serious intercurrent illness or infection
  • Known coagulation disorders
  • Emergencies
Both
18 Years to 89 Years
No
Contact: Alessandro Parolari, MD, PhD 00390258002558 alessandro.parolari@ccfm.it
Italy
 
NCT00755248
BAPPY
No
Centro Cardiologico Monzino
Centro Cardiologico Monzino
Not Provided
Principal Investigator: Alessandro Parolari, MD, PhD Centro Cardiologico Monzino - Milano
Centro Cardiologico Monzino
September 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP