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Real-World Study: Clinical Efficacy and Safety of Vericiguat Treatment in Patients with Heart Failure in the Vulnerable Phase

Real-World Study: Clinical Efficacy and Safety of Vericiguat Treatment in Patients with Heart Failure in the Vulnerable Phase

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097846
Enrollment
Unknown
Registered
2025-02-26
Start date
2024-05-16
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Heart Failure

Interventions

Vericguat treatment group:None

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Fully understand the purpose and requirements of this study, sign the informed consent form, and have good compliance. 2. Participants who meet the following conditions: (1). Participants aged 18 and above; (2). Have been clearly diagnosed with heart failure, meet the diagnostic criteria for heart failure, NYHA>=II level; (3). Received Vericiguat treatment during 2021-2024, and the treatment time is not less than 1 month; (4). Can provide complete medical records, including treatment plans, medication information, clinical course, etc.

Exclusion criteria

Exclusion criteria: 1.Participants who have undergone heart transplantation or are waiting for heart transplantation; 2.Participants with severe end-stage organ diseases, such as severe liver and kidney failure, etc. 3.Participants with severe other cardiovascular events, such as acute coronary syndrome, stroke, etc. 4.Participants with active cancer or undergoing cancer treatment; 5.Participants with severe immune system diseases, such as systemic lupus erythematosus, rheumatoid arthritis, etc. 6.Participants with severe mental illness or cognitive impairment, affecting treatment compliance and data collection capabilities; 7.Participants who have received other clinical trial treatments within 3 months before the start of the study; 8.Participants who are allergic to Vericiguat or related drugs; 9.Participants using other sGC stimulants; 10.Participants who cannot provide complete medical records or key information.

Design outcomes

Primary

MeasureTime frame
NT-proBNP;LVEF;LVDd;NYHA class;Main outcome events (Emergency treatment due to heart failure, readmission due to heart failure, death due to heart failure, and all-cause mortality events);

Secondary

MeasureTime frame
All-cause mortality;Blood Pressure;Creatinine;

Countries

China

Contacts

Public ContactAilan Chen

The First Affiliated Hospital of Guangzhou Medical University

1228327958@qq.com+86 20 83062748

Outcome results

None listed

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