Effect of Left Ventricle Diastolic Dysfunction on Outcomes in Female Cardiac Surgery Patients
Recruiting · NCT05972356 · Observational (researchers observe without assigning treatment) · Lead sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
View the official record on ClinicalTrials.gov →What this trial is about
The aim of this study is to evaluate the differences between males and females with LVDD, undergoing cardiac surgery. The investigators will look at perioperative factors such as body weight, body surface area, previous medical history, cardiac function measured by amongst others, transoesophageal echocardiography and haemodynamic parameters, transfusion, coagulation, cardiopulmonary bypass (CPB) related factors, inotropic requirements, risk, and outcome scores as well as complications, morbidity and mortality at 30 days. The investigators will evaluate these variables in an observational setting, with the goal of improving outcome in females after cardiac surgery in the future.
Who can take part
Inclusion criteria
- All patients \>18 years, who undergo cardiac surgery from 1 January 2023 till 31 December 2026 in the Amsterdam UMC
Exclusion criteria
- Patients who object to the re-use of their care data
Where it is running
1 location listed.
- Academic Medical Center - Amsterdam, North Holland, Netherlands