Ireland
--:--IST
Recruiting Not applicable

Angiopoietin and Adverse Outcomes in Cardiac Surgery

NCT05817929 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-03-23
Last updated
2025-05-25

Condition(s) studied

Cardiac SurgeryAcute Kidney Injury

Investigational drug(s) / intervention(s)

blood sample

blood sample: 5 ml blood sample will be withdrawn at the surgery start and at the surgery end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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * adult patient scheduled for cardiac surgery under cardiopulmonary bypass Exclusion Criteria: * patient less than 18 years old, * redo surgery, * urgent surgery, * endocarditis, * aortic root repair surgery * aortic dissection * heart beating surgery, * heart transplantation

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)

FacilityCityRegionStatus
CHU Amiens Picardie Amiens France Recruiting
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 NCT05817929 on ClinicalTrials.gov ↗ ← All trials in France