Comparing the Efficacy and Safety of Vericiguat With Standard Medical Treatment in Heart Failure Patients

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-80
SponsorNational Institute of Cardiovascular Diseases, Pakistan

About this trial

To compare the effectiveness and safety of Vericiguat with Standard Medical Treatment in Patients with Heart Failure and Reduced Ejection Fraction

Eligibility criteria

Qualifiers

Age >18 years of any gender

Chronic heart failure (New York Heart Association [NYHA] functional class II, III, or IV), a reduced left ventricular ejection fraction of less than 45% within 12 months before randomization

Elevated natriuretic peptide level: (For patients in sinus rhythm, the criteria include a plasma B-type natriuretic peptide (BNP) level of at least 300 pg per milliliter or an NT-proBNP level of at least 1000 pg per milliliter. For patients in atrial fibrillation, the criteria included a BNP level of at least 500 pg per milliliter or an NT-proBNP level of at least 1600 pg per milliliter).

Evidence of worsening heart failure.

Disqualifiers

Systolic blood pressure of less than 100 mm Hg.

Concurrent or anticipated use of long-acting nitrates.

Use of intravenous inotropes or implantable left ventricular assist devices.

Not on standard of care medical treatment for heart failure.

Trial design

Treatments tested in this trial

  • Vericiguat tablet
  • Placebo

Treatment groups

500 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators