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The effect of allopurinol on the prognosis of patients with acute myocardial infarction with hyperuricemia

The effect of allopurinol on the prognosis of patients with acute myocardial infarction with hyperuricemia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024152
Enrollment
Unknown
Registered
2019-06-28
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-07-01

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

Conditions

acute myocardial infarction with hyperuricemia

Interventions

placebo group:placebo

Sponsors

Xiamen Cardiovascular Hospital Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) patients aged 18 to 75 years who were diagnosed as acute myocardial infarction according to symptoms of ischemic chest pain, changes in electrocardiogram and markers of myocardial injury; 2) serum uric acid greater than 7.0mg/dL with or without goutserum uric acid greater than 6mg/dL with gout; 3) the subjects can understand and comply with the protocol requirements, including regular clinical follow-up; 4) subject's legal representative is able and willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1) pregnant patients; 2) patients with contraindication to allopurinol, e.g. hypersensitivity to this product, severe liver and kidney dysfunction, and low blood cells; 3) the patient had received uric acid lowering treatment within 30 days prior to screening (such as allopurinol, febulatol, promethazone, etc.); 4) active peptic ulcer disease; 5) liver transaminase was more than 3 times the normal value; 6) creatinine clearance rate was less than 30ml/min; 7) the patient had a history of malignant tumor within 5 years; 8) patients with myocardial infarction 60 days before screening;

Design outcomes

Secondary

MeasureTime frame
transient ischemic attack;Hospitalized CHF;Arrhythmias not associated with ischemia;Venous and peripheral arterial thromboembolic events;

Primary

MeasureTime frame
CV death;Nonfatal MI;Nonfatal stroke;Unstable angina with urgent coronary revascularization;

Countries

China

Contacts

Public ContactZhu Weiliang

Xiamen Cardiovascular Hospital Xiamen University

dimtarget@163.com+86 15711568281

Outcome results

None listed

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