Registry to improve outcomes after heart and chest surgeries
Registry for the Improvement of Postoperative OutcomeS in Cardiac and Thoracic surgEry
This study is collecting information from patients who have heart and chest surgeries to see how different factors affect their recovery and overall outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 8000 (estimated) |
| Sex | All |
| Sponsor | CMC Ambroise Paré Academic / other |
| Locations | 1 site (Neuilly-sur-Seine, Île-de-France Region) |
| Trial ID | NCT03209674 on ClinicalTrials.gov |
What this trial studies
This registry aims to collect data on patients undergoing cardiac and thoracic surgeries to analyze the relationship between various preoperative and intraoperative factors and their postoperative outcomes. By gathering information on patient characteristics, surgical details, and complications, the study seeks to enhance understanding of factors that contribute to morbidity and mortality in these surgeries. The goal is to improve perioperative care and ultimately patient outcomes in cardiac and thoracic surgery.
Who should consider this trial
Good fit: Ideal candidates for this registry are all patients who are eligible for cardiac or thoracic surgery.
Not a fit: Patients who are not eligible for cardiac or thoracic surgery will not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could lead to improved postoperative care and reduced complications for patients undergoing cardiac and thoracic surgeries.
How similar studies have performed: Other studies have shown success in using registries to improve surgical outcomes, indicating that this approach is both valid and beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * all patients eligible for cardiac or thoracic surgery Exclusion Criteria: * non applicable
Where this trial is running
Neuilly-sur-Seine, Île-de-France Region
- CMC Ambroise Paré — Neuilly-sur-Seine, Île-de-France Region, France (Recruiting)
Study contacts
- Study coordinator: Alain Brusset, MD
- Email: brusseta@club-internet.fr
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.