Registry for the Improvement of Postoperative OutcomeS in Cardiac and Thoracic surgEry

NCT03209674 · tracked via the Priya Life Science France tracker

Sponsor

CMC Ambroise Paré

Phase

Observational

Started

2012-01-01

Last updated

2026-04-03

Condition(s) studied

Heart DiseasesDeathPostoperative ComplicationsCardiac Complication

Investigational drug(s) / intervention(s)

Cardiothoracic surgery

Cardiothoracic surgery: Cardiac or thoracic procedure

Study summary

The registry for the improvement of postoperative outcomes in cardiac and thoracic surgery aims to prospectively collect data in order to test the association between various preoperative and per-operative variables ; and several postoperative outcomes such as mortality, shock, redo surgery, sepsis and extracorporeal life-support.

Eligibility

Sex

ALL

Min age

—

Max age

—

Healthy volunteers

Inclusion Criteria: * all patients eligible for cardiac or thoracic surgery Exclusion Criteria: * non applicable

Primary outcome measure(s)

In-hospital mortality — During follow-up, until discharge from hospital, up to 1 year.
death occurring in the same hospital where the operation took place before discharge from the hospital

Trial sites (1)

Facility	City	Region	Status
CMC Ambroise Paré	Neuilly-sur-Seine	Île-de-France Region	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03209674 on ClinicalTrials.gov ↗ ← All trials in France