Review of patient outcomes after coronary artery bypass grafting
Enhancing Care in Patients After Coronary Artery Bypass Graft Surgery (CABG)： OptiCABG Study
Chinese Academy of Medical Sciences, Fuwai Hospital · NCT06488352
This study looks at the experiences of patients who had heart surgery to see how they did afterward and what factors might affect their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 40000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Chinese Academy of Medical Sciences, Fuwai Hospital (other) |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Trial ID | NCT06488352 on ClinicalTrials.gov |
What this trial studies
This observational study reviews data from patients who underwent coronary artery bypass grafting (CABG) at Fuwai Hospital over a ten-year period. It aims to analyze medical histories, postoperative complications, and outcomes such as mortality and arrhythmias. The study will utilize case-control and retrospective cohort methodologies to identify risk factors associated with early postoperative complications and develop predictive models for patient management.
Who should consider this trial
Good fit: Ideal candidates are patients who have undergone CABG between January 2013 and June 2023.
Not a fit: Patients who were discharged within 72 hours of admission or had emergency CABG surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve postoperative care and outcomes for patients undergoing CABG.
How similar studies have performed: Other studies have shown success in identifying risk factors for postoperative complications in cardiac surgery, making this approach relevant and potentially impactful.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients accepted CABG enrolled from January 2013 to June 2023 Exclusion Criteria: * patients discharged within 72 hours of admission * patients with an admission diagnosis of atrial fibrillation * patients underwent CABG as emergency surgery * patients underwent concurrent surgical treatments * patients with repeat admissions
Where this trial is running
Beijing, Beijing Municipality
- Structral Heart Disease Center, Fuwai Hospital — Beijing, Beijing Municipality, China (RECRUITING)
Study contacts
- Principal investigator: Xiangbin Pan, MD — Chinese Academy of Medical Sciences, Fuwai Hospital
- Study coordinator: Ziping Li, MD
- Email: ziping_li@yeah.net
- Phone: 88396666
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.
Conditions: Coronary Artery Bypass