Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06768528

Association Between GalectiN-3 and POSt-operative AtrIal Fibrillation After Coronary Artery BypaSs Graft

Association Between Galectin-3 and Post-operative AtrIal Fibrillation After Coronary Artery Bypass Graft

Status
Recruiting
Phase
Study type
Observational
Enrollment
90 (estimated)
Sponsor
University of Sao Paulo General Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational study is to test the association between high levels of Galectin-3 and the occurrence of post-operative atrial fibrillation after isolated coronary artery bypass grafting (CABG). The main question\[s\] it aims to answer are: * Is Galectin-3 an accurate biomarker to predict higher risk of developing post-operative atrial fibrillation? * Are high levels of Galectin-3 associated to other post-operative complications and major adverse cardiovascular events? Participants will be enrolled during pre-operative evaluation and a peripheral blood sample collection will be performed in the 24h before CABG. Participants will then be followed for a period of 12 months (daily during hospitalization and 3 appointments after hospital discharge) to determine whether patients with higher levels of Galectin-3 will have worse outcomes.

Detailed description

Prospective, observational, single-center cohort study including patients undergoing coronary artery bypass graft (CABG) surgery. Patients will be enrolled during preoperative evaluation. A peripheral blood sample will be collected within 24 hours before surgery and patients will be followed during hospitalization and for 12 months after discharge.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTGalectin-3 dosagePeripheral blood sample will be collected in the 24h before CABG

Timeline

Start date
2023-01-01
Primary completion
2025-02-28
Completion
2026-12-01
First posted
2025-01-10
Last updated
2025-01-10

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT06768528. Inclusion in this directory is not an endorsement.