Angiopoietin and Adverse Outcomes in Cardiac Surgery
Condition(s) studied
Investigational drug(s) / intervention(s)
blood sample: 5 ml blood sample will be withdrawn at the surgery start and at the surgery end
Study summary
Cardiac surgery and cardiopulmonary bypass can lead to systemic organ failure trough excess inflammation and endothelial injury. The angiopoietin family represented by angiopoietin 1 and 2 can reflect endothelial injury by a decrease in angiopoietin 1 and an increase in angiopoietin 2. The investigators hypothesized that angiopoietin dysregulation could reflect organ failure related to cardiac surgery.
The purpose of this project is to assess the association between angiopoietin dysregulation and adverse outcomes on cardiac surgery.
Eligibility
Primary outcome measure(s)
- Correlation between abnormal angiopoietin 1 concentration (ng/ml) and number of major cardiovascular event — 28 days
major cardiovascular event are myocardial infraction, stroke, acute kidney injury, cardiovascular death - correlation between occurence of abnormal angiopoietin 2 concentration (ng/ml) and occurence of major cardiovascular event — 28 days
major cardiovascular event are myocardial infraction, stroke, acute kidney injury, cardiovascular death
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU Amiens Picardie | Amiens | France | Recruiting |
More Centre Hospitalier Universitaire, Amiens trials in France
Other trials for the same condition
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 NCT05817929 on ClinicalTrials.gov ↗ ← All trials in France