Actively Recruiting

Age: 18Years +
All Genders
NCT05972356

Effect of Left Ventricle Diastolic Dysfunction on Outcomes in Female Cardiac Surgery Patients

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2026-02-17

1000

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

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.

CONDITIONS

Official Title

Effect of Left Ventricle Diastolic Dysfunction on Outcomes in Female Cardiac Surgery Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years and older
  • Patients undergoing cardiac surgery at Amsterdam UMC between January 1, 2023 and December 31, 2026
Not Eligible

You will not qualify if you...

  • Patients who do not allow their medical care data to be used for research

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Academic Medical Center

Amsterdam, North Holland, Netherlands, 1105AZ

Actively Recruiting

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Research Team

J

Jennifer Breel, MSc,PhD

CONTACT

S

Susanne Eberl, MD,PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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