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NCT07830940Not yet recruitingPhase 4

Finerenone and Cardiac Remodeling in HFpEF

Impact of Finerenone on Cardiac Remodeling and Heart Failure Progression in Patients With Heart Failure With Preserved Ejection Fraction The FIN-HF-LVS Registry

Source: ClinicalTrials.gov · Last updated 22 Sept 2026

Brief summary (registry, in English)

This prospective randomized study aims to evaluate the efficacy of Finerenone as add-on therapy to standard of care compared to standard of care alone in preventing heart failure worsening and preserving cardiac function assessed by left ventricular strain in patients with heart failure with preserved ejection fraction.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
194 (estimated)
First submitted
15 Sept 2026
Start date
20 Sept 2026
Primary completion date
25 Sept 2027
Lead sponsor
Assiut University
NCT number
NCT07830940

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 194
  • From 20 Sept 2026 to the primary completion date, 25 Sept 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Implanted cardiac pacemaker or defibrillator with active atrial pacing
  • Known hypersensitivity to Finerenone

Lab values

  • Baseline serum potassium greater than 5 milliequivalents per liter

Other

  • Estimated glomerular filtration rate less than 25 milliliters per minute per 1.73 square meters

Who the study is looking for

  • Age greater than or equal to 18 years
  • Clinically evidenced heart failure with left ventricular ejection fraction greater than or equal to 50 percent
  • HFA-PEFF score greater than or equal to 5 or score 2 to 4 with functional testing confirming HFpEF
  • Sinus rhythm on resting ECG at screening
  • Written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.