Skip to content

Plasma Biomarkers in Cardiac Valve Surgery

Measurement of Four Plasma Biomarkers for Risk Stratification and Determination of Functional Recovery After Cardiac Valve Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02641665
Enrollment
250
Registered
2015-12-29
Start date
2016-01-31
Completion date
2018-12-31
Last updated
2017-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Elective Valvular Cardiac Surgery

Brief summary

The level of four biomarkers will be measured in the patients' plasma after induction of anaesthesia. There biomarkers are NT-ProBNP, ST2, Galectin-3 and GDF-15. The level of these marker will then be correlated with early (30 days) and late (one year) patients' prognosis and with functional recovery (MLHFQ score).

Interventions

Aortic or mitral valve replacement/repair performed in isolation of in addition to coronary artery bypass graft(s).

Sponsors

University of Liege
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Elective/urgent aortic or mitral valve surgery in isolation or combined with CABG

Exclusion criteria

* Emergency or salvage surgery * Inability to consent * Previous cardiac surgery * Stage IV or V CDK (GFR ≤ 30 ml/min) or dialysis * Active Endocarditis * Liver cirrhosis * Chronic atrial fibrillation * Pacemaker

Design outcomes

Primary

MeasureTime frameDescription
Composite primary outcome30 daysIn hospital or 30-days mortality or inotropic support during more than 48 hours or lengthy of ICU stay longer than 5 days

Secondary

MeasureTime frameDescription
Post-operative AKI48 hoursAKIN stage during the first 48 hours
Ejection fraction1 yearEF at 30 days and at 1 year
NYHA1 yearNYHA class at 30 days and at 1 year
ICU readmission30 days
reshopitalisation1 yearhospital admission for cardiac failure during the first postoperative year
one year mortality1 yearmortality during the first postoperative year.
MLHFQ1 yearMinnesota living with heart failure questionnaire at 30 days and at 1 year

Countries

Belgium

Contacts

Primary ContactGregory A Hans, MD, PhD
G.Hans@chu.ulg.ac.be+3243667655

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026