Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06399627

Effect of Non-anemic Iron Deficiency on Outcome Following Off-pump Coronary Revascularization

Status
Recruiting
Phase
Study type
Observational
Enrollment
433 (estimated)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
29 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This is a single center retrospective study of patients who underwent off pump coronary artery bypass surgery between 2016.11\~2023.05. From this patient group, preoperatively non-anemic patients were selected and were divided into 2 cohorts according to their preoperative iron status; iron replete and iron deficient. These two cohorts were compared to evaluate the effect of preoperative iron deficiency on patient outcomes. The primary end point was the occurrence of composite morbidity/mortality end points which were: in hospital mortality, acute kidney injury (AKI), stroke, deep sternal infection, hemostatic reoperation, prolonged mechanical ventilation of more than 24hours, delirium and postoperative myocardial infarction. Occurrence of any one of these outcomes counted as primary end point met. Secondary outcome was to evaluate and compare hemoglobin recovery of iron replete and deficient patients until one year after surgery.

Conditions

Timeline

Start date
2016-11-01
Primary completion
2024-05-31
Completion
2024-05-31
First posted
2024-05-06
Last updated
2024-05-06

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06399627. Inclusion in this directory is not an endorsement.