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Safety and efficacy of Vericiguat 5mg initiation in combination with guideline-directed medical therapy in the treatment of Heart failure with reduced ejection fraction

Safety and efficacy of Vericiguat 5mg initiation in combination with guideline-directed medical therapy in the treatment of Heart failure with reduced ejection fraction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116645
Enrollment
Unknown
Registered
2026-01-13
Start date
2025-04-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Heart failure

Interventions

Observation Group for Heart Failure treatment:None

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 85 years old, clinically diagnosed with HFrEF (left ventricular ejection fraction LVEF =4 weeks (including at least two of the quadruple drugs of ARNI/ACEI/ARB, beta-blockers, MRA and SGLT2i) 3. Baseline systolic blood pressure >=85 mmHg and no severe hemodynamic instability

Exclusion criteria

Exclusion criteria: 1. Acute myocardial infarction, stroke or cardiogenic shock has occurred within the past three months; 2. Severe liver and kidney dysfunction (eGFR 3 times the upper limit of normal); 3. Known to be allergic to or have contraindications to viliciqua; 4. Patients with an expected lifespan of less than one year; 5. Survivors of cardiac arrest remain in a coma. 6. Severe bradycardia or tachycardia; 7. Patients with shock caused by pulmonary embolism or pericardial tamponade; 8. Hypertrophic cardiomyopathy; 9. Moderate to severe aortic insufficiency; 10. Aortic dissection, moderate to severe aortic reflux; 11. Uncontrollable bleeding within the past six months; 12. Patients with malignant tumors or those with serious diseases such as malignant tumors, with an expected lifespan of less than one year; 13. Pregnant and lactating women; 14. Neuropsychiatric disorders, unable to cooperate with management; 15. Participated in other clinical trials in the past year; 16. Other circumstances that the researcher deems unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
14-day dose compliance rate;Absolute improvement in left ventricular ejection fraction (LVEF) at 20 weeks compared to baseline (%);

Secondary

MeasureTime frame
All-cause mortality;Readmission rate for heart failure;

Countries

China

Contacts

Public ContactWushi Wang

The First Hospital of Jilin University

yushi@jlu.edu.cn+86 431 8878 2417

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026