Prior CABG Patients Evaluated for Saphenous VeIn grAft DysfUnction and Progression of Coronary arTery Disease
Recruiting · NCT04772768 · Observational (researchers observe without assigning treatment) · Lead sponsor: Amsterdam UMC, location VUmc
View the official record on ClinicalTrials.gov →What this trial is about
This is a multi-center, observational cohort study including patients with prior coronary artery bypass grafting (CABG) and ≥1 saphenous vein grafts (SVG) presenting with recurrent ischemic symptoms. Objective: to investigate the clinical outcomes in patients with prior CABG evaluated for bypass graft failure and progression of native coronary artery disease (CAD). Follow-up will be collected through national registry databases, electronic medical patient records and standardized telephonic assessment at 3 and 5 years follow-up.
Who can take part
Age range
18 Years to 90 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Prior coronary artery bypass grafting
- One or more saphenous vein grafts
- Recurrent angina symptoms
Exclusion criteria
- \<18 years of age
- ≥ 90 years of age
- Cardiogenic shock
- Pregnancy
- Failure to provide informed consent
Where it is running
1 location listed.
- Amsterdam University Medical Centers, Department of Cardiology - Amsterdam, Netherlands