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Vericiguat for Heart Failure With Reduced Ejection Fraction After Myocardial Infarction

Vericiguat for Ventricular Remodeling in Patients With Heart Failure With Reduced Ejection Fraction After Myocardial Infarction

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06717204
Acronym
HFrEF
Enrollment
210
Registered
2024-12-04
Start date
2025-01-01
Completion date
2027-12-31
Last updated
2024-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HFrEF - Heart Failure With Reduced Ejection Fraction, Myocardial Infarction (MI)

Keywords

HFrEF, Myocardial Infarction, Vericiguat

Brief summary

The effects of vericiguat on cardiac remodeling in patients with chronic stable heart failure after myocardial infarction have not been reported. This project aims to clarify the efficacy and safety of vericiguat in patients with chronic heart failure after myocardial infarction. Patients with chronic stable heart failure with reduced ejection fraction after myocardial infarction in the electronic medical records of Qilu Hospital of Shandong University will be selected and divided into two groups: the treatment group received vericiguat in addition to conventional treatment and the control group received conventional treatment only. After 12-month treatment, the effects of vericiguat on cardiac remodeling and function and cardiovascular adverse events will be evaluated. The results are helpful to provide a new treatment strategy for chronic heart failure after myocardial infarction.

Interventions

DRUGVericiguat Oral Tablet [Verquvo]

Vericiguat in addition to conventional treatment

Conventional treatment only

Sponsors

Jinan Central Hospital
CollaboratorOTHER
Qianfoshan Hospital
CollaboratorOTHER
Qilu Hospital of Shandong University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. The history of acute myocardial infarction exceeds 3 months; 2. Symptoms and signs of heart failure have been stable for more than one month; 3. 18 years old or more; 4. NYHA cardiac function classified as grade II\ IV; 5. LVEF≤40%; 6. NT-proBNP≥450pg/ml; 7. All subjects or their guardians must sign the subject consent before entering the trial.

Exclusion criteria

1. Patients with the following diseases: nonischemic cardiomyopathy; valvular heart disease; congenital heart disease; obstruction of left ventricular outflow tract; severe decompensated heart failure; active myocarditis or pericardial disease; end-stage liver and kidney diseases; malignant tumor; 2. Mechanical complications of myocardial infarction; 3. Unable to obtain primary outcome data.

Design outcomes

Primary

MeasureTime frameDescription
LVEDVI=LVEDV/BSAFrom baseline to the end of 12-month treatmentChanges of left ventricular end-diastolic volume index (LVEDVI) compared with baseline after 12 months

Countries

China

Contacts

Primary ContactPanpan Hao, MD, PhD
panda.how@sdu.edu.cn86-18560086593

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026