Skip to content

Serum uric acid change after oral inosine administration

Serum uric acid change after oral inosine administration

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061080
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Hyperuricemia

Interventions

control group:orally take inosine tablets for 500mg
hyperuricemia group:orally take inosine tablets for 500mg

Sponsors

Shanghai 10th People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male, Han nationality, aged 18-70 years; 2.(eGFR) > 60 mL/min/1.73m2; 3. Voluntary informed consent and participation.

Exclusion criteria

Exclusion criteria: 1. Using drugs affecting uric acid metabolism, such as allopurinol, fibulinastat, benzbromarone, atorvastatin, losartan, amlodipine, fenofibrate, pyrazinamide, diuretics, glucocorticoids, immunosuppressants, aspirin, etc.; 2. With malignant tumor, immune system disease, blood disease, tuberculosis and other related concomitant diseases; 3. Patients with uncontrolled hypertension, systolic blood pressure >= 180 and/or diastolic blood pressure >= 110 mmhg; 4. With abnormal glucose metabolism: fasting blood glucose > 10 mmol/L, and/or glycosylated hemoglobin >= 9%; 5. With abnormal liver and kidney function: patients with severe liver dysfunction (ALT and AST >= 2.5unl), patients with acute or chronic renal failure (EGFR < 30 ml/min).

Design outcomes

Primary

MeasureTime frame
uric acid;inosine;

Secondary

MeasureTime frame
creatine;total cholesterol;triglyceride;glucose;Alanine aminotransferase;Aspartate aminotransferase;height;weight;

Countries

China

Contacts

Public ContactChen Haibing

Shanghai 10th People’s Hospital

18930173813@163.com+86 18930173813

Outcome results

None listed

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