RecruitingNot ApplicableNCT07341893

Sacubitril-valsartan in Patients With Heart Failure.

Clinical Study Evaluating Efficacy and Safety Sacubitril-valsartan in Patients With Heart Failure.


Sponsor

Damanhour University

Enrollment

60 participants

Start Date

Aug 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of this study is to evaluate the safety and efficacy of Sacubitril -Valsartan in patients with heart failure.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study is evaluating the effectiveness of sacubitril-valsartan (Entresto), a heart failure medication, in patients with heart failure and reduced pumping function (reduced ejection fraction). It tracks whether the drug improves heart function and reduces symptoms over time. **You may be eligible if...** - You are 18 or older - You have heart failure with a reduced ejection fraction (the heart pumps out 40% or less of blood with each beat) - Your heart failure symptoms are NYHA class II–IV (ranging from mild symptoms on exertion to symptoms at rest) **You may NOT be eligible if...** - You have severe kidney disease (GFR below 20 mL/min) - Your blood potassium is dangerously high (above 5.5 mmol/L) - You are pregnant or breastfeeding - You have an active infection - You have congenital (birth-related) heart disease, an autoimmune or connective tissue disorder, or severe liver disease Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSacubitril-valsartan

patients (n=30) will be given Sacubitril-valsartan 50 mg twice daily.

DRUGstandard treatment of heart failure

Control group (n=30) on standard treatment of heart failure.


Locations(1)

Damanhur Medical National Institute

Damanhūr, Elbehairah, Egypt

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NCT07341893


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