Collecting data on outcomes after coronary artery bypass grafting
E-CABG: European Multicenter Study on the Outcome After Coronary Artery Bypass Grafting
This study is collecting information from patients who have heart surgery to see how different factors and treatments affect their recovery and overall outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 4000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Oulu Academic / other |
| Locations | 1 site (Oulu) |
| Trial ID | NCT02319083 on ClinicalTrials.gov |
What this trial studies
The E-CABG registry is a multicenter initiative across Europe that gathers data on patients undergoing isolated coronary artery bypass grafting (CABG). This observational study aims to collect comprehensive information on preoperative characteristics, treatment strategies, and postoperative outcomes from various cardiac surgery centers. By analyzing data from diverse patient populations, the study seeks to evaluate the impact of different risk factors and the effectiveness of surgical methods and medications used during the entire treatment process. The findings will contribute to improving surgical practices and patient care in coronary artery disease.
Who should consider this trial
Good fit: Ideal candidates for this study are patients over 18 years old who are undergoing isolated CABG for stable coronary artery disease or acute coronary syndrome.
Not a fit: Patients undergoing any other major cardiac surgery procedures will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of CABG outcomes and lead to improved treatment strategies for patients with coronary artery disease.
How similar studies have performed: Other studies have shown success in utilizing multicenter registries to improve surgical outcomes, making this approach both validated and promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients of aged \> 18 years undergoing isolated CABG for stable coronary artery disease or acute coronary syndrome. Patients undergoing Maze procedure will be included in this registry. Exclusion Criteria: * Patients undergoing any other major cardiac surgery procedure will be excluded from this registry.
Where this trial is running
Oulu
- Oulu University Hospital — Oulu, Finland (Recruiting)
Study contacts
- Study coordinator: Fausto Biancari, Professor
- Email: faustobiancari@yahoo.it
- Phone: +358407333973
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.