Registry to improve outcomes after heart and chest surgeries
Official title: Registry for the Improvement of Postoperative OutcomeS in Cardiac and Thoracic surgEry
Run by CMC Ambroise Paré · NCT03209674 · Data updated 2026-11-12
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 |
|---|---|
| Sex | All |
| Enrollment | 8000 (estimated) |
| Sponsor | CMC Ambroise Paré Academic / other |
| Locations | 1 site (Neuilly-sur-Seine, Île-de-France Region) |
| Status | Recruiting |
| Started | January 1, 2012 |
| Main results expected | December 31, 2030 |
| Study ends | December 31, 2030 |
| Registry record updated | April 3, 2026 |
| Trial ID | NCT03209674 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this registry are all patients who are eligible for cardiac or thoracic surgery.
✕Probably not a fit
Patients who are not eligible for cardiac or thoracic surgery will not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: Other studies have shown success in using registries to improve surgical outcomes, indicating that this approach is both valid and beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * all patients eligible for cardiac or thoracic surgery Exclusion Criteria: * non applicable
Where it's running
-
CMC Ambroise Paré
Neuilly-sur-Seine, Île-de-France Region, France Recruiting
Study contacts
- Study coordinator: Alain Brusset, MD
- Email: brusseta@club-internet.fr
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.