Evaluating complications and mortality after cardiac surgery
Evaluation of Post-operative Morbidity and Mortality After Cardiac Surgery Performed in Bichat Hospital
This study looks at the risks and outcomes for adults who have heart surgery using a heart-lung machine to see how their health is affected during their hospital stay.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 12000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT03393169 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess in-hospital morbidity and mortality rates following cardiac surgeries performed under extracorporeal circulation at Bichat Hospital. It involves a comprehensive database that records preoperative patient characteristics, types of surgeries, postoperative complications, and in-hospital mortality. The study seeks to analyze these outcomes in relation to patient characteristics and surgical interventions, providing valuable insights into the risks associated with cardiac surgery. It is a prospective, monocentric study focusing on adult patients aged 18 and older who consent to the recording of their medical data during hospitalization.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older undergoing cardiac surgery with extracorporeal circulation.
Not a fit: Patients who are under 18 years old or do not consent to the recording of their medical data may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of postoperative risks, leading to improved patient outcomes in cardiac surgery.
How similar studies have performed: Other studies have shown success in evaluating postoperative outcomes in cardiac surgery, indicating that this approach is supported by existing research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years and older and has legal capacity - cardiac surgery under extra corporeal circulation * non objection to record medical information during hospitalization Exclusion Criteria: \-
Where this trial is running
Paris
- département de cardiologie et d'anesthésie réanimation Hôpital Bichat 46 rue Henri Huchard — Paris, France (Recruiting)
Study contacts
- Study coordinator: Bernard IUNG, MD.
- Email: bernard.Iung@aphp.fr
- Phone: 01 40 25 66 01
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.