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RECRUITINGOBSERVATIONAL

Effect of Pre-Hospital ARNI Therapy on Short-Term Outcomes in HFrEF

Evaluating the Impact of Pre-Hospital Angiotensin Receptor-Neprilysin Inhibitor (ARNI) Therapy on Short-Term Clinical Outcomes in Heart Failure Patients With Reduced Ejection Fraction: A Comparative Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This study looks at people with heart failure who are admitted to the hospital. The goal of the study is to understand whether taking a heart failure medicine called angiotensin receptor-neprilysin inhibitor (ARNI) before hospital admission affects short-term health outcomes. The study will compare two groups of participants: those who were already taking ARNI before coming to the hospital and those who were not. Information will be collected from medical records during the hospital stay, including heart-related events, kidney-related events, and how long participants stay in the hospital. Some participants will also be followed for a short period after discharge. This study may help improve understanding of outcomes associated with ARNI use in people with heart failure in routine clinical care.

Who May Be Eligible (Plain English)

Who May Qualify: - \>= 18 years, male or female EF \<40% Who Should NOT Join This Trial: - EF\>40% Pregnancy or breastfeeding Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * \>= 18 years, male or female EF \<40% Exclusion Criteria: * EF\>40% Pregnancy or breastfeeding

Treatments Being Tested

OTHER

Prehospital ARNI use

Participants who were using ARNI therapy before hospital admission

OTHER

No prehospital ARNI use

Participants who were not using ARNI therapy before hospital admission

Locations (1)

Mansoura university Hospital
Al Mansurah, Egypt