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An Interventional study on the impact of hyperuricaemia on the prognosis of patients with heart failure with preserved ejection fraction.

A prospective, randomised, parallel, controlled interventional study on the impact of hyperuricaemia on the prognosis of patients with heart failure with preserved ejection fraction.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110728
Enrollment
Unknown
Registered
2025-10-20
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Heart failure, Hyperuricemia

Interventions

Group A:Benzbromarone 50mg-100mg once daily.
Group B:Allopurinol 50-100mg twice to thrice daily

Sponsors

The Third People's Hospital of Chengdu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Hospitalised patients with heart failure aged 18 years or older; 2) The diagnostic criteria for heart failure according to the 2021 and 2023 European Society of Cardiology "Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure" and its updates, as well as the "Chinese Guidelines for the Diagnosis and Treatment of Heart Failure 2018" regarding symptoms, signs, and serum biomarkers of heart failure; 3) Left ventricular ejection fraction >= 50%, NYHA heart function class II-IV; 4) Diagnostic standards for hyperuricaemia based on the 2017 "Practical Guidelines for the Diagnosis and Treatment of Hyperuricaemia in Chronic Kidney Disease" and the 2020 "Practice Guidelines for Patients with Hyperuricaemia/Gout", with uric acid levels in the past three months being male >= 420umol/L and female >= 360umol/L; 5) Voluntary participation in the trial and signing of informed consent.

Exclusion criteria

Exclusion criteria: The following conditions will exclude this trial: 1) Those who have not signed the informed consent form or have poor compliance; 2) Individuals with severe liver or kidney dysfunction, ALT/AST/ total bilirubin greater than 3 times the normal upper limit; eGFR < 30 mL/(min.1.73 m²); 3) Those with a left ventricular ejection fraction < 50%; 4) Patients with severe gout or poor response to medication; 5) Female subjects who are pregnant, breastfeeding, or have a positive pregnancy test; 6) Patients with a confirmed diagnosis of malignant tumors during the screening inclusion period or intervention follow-up period; 7) Those who have undergone or are expected to undergo ventricular de-synchronization treatment or left ventricular assist device placement within 3 months; 8) Individuals with a confirmed diagnosis of urinary system stones that have not been treated; 9) Individuals who have had an acute gout attack within the last month; 10) Patients with contraindications to the study intervention medication; 11) Those diagnosed with peripartum or chemotherapy-induced cardiomyopathy within 3 months prior to the screening inclusion period; 12) Those with acute coronary syndrome, stroke, transient ischaemic attack, or major surgeries on the heart or carotid artery such as coronary artery bypass grafting, percutaneous coronary intervention, or carotid angioplasty within 3 months prior to the screening inclusion period.

Design outcomes

Primary

MeasureTime frame
All cause death or Cardiovascular death ;Heart failure rehospitalization;

Secondary

MeasureTime frame
Control rate of Hyperuricemia;

Countries

China

Contacts

Public ContactJunbo Xu

The Third People's Hospital of Chengdu

xujunbo2000@sina.com+86 28 6131 2288

Outcome results

None listed

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