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Renal protective effect of intravenous alkalization therapy on patients with chronic kidney disease complicated with hyperuricemia

Renal protective effect of intravenous alkalization therapy on patients with chronic kidney disease complicated with hyperuricemia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061029
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

chronic kidney disease with hyperuricemia

Interventions

Pre-stage control treatment::Saline, intravenous * 5 days
Post-stage trial treatment:Post trial treatment: 5% sodium bicarbonate solution, 1meq/kg body weight, intravenous for 5 days

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years, Han nationality and unlimited gender; ? Glomerular filtration rate (eGFR) 30-60 ml/min/1.73m2 or GFR >= 60ml/min/1.73m2, combined with proteinuria and renal imaging changes; ? Hyperuricemia with blood uric acid >= 420umol/L.

Exclusion criteria

Exclusion criteria: 1. eGFR<30ml/min/1.73m2; 2. Abnormal liver function, with alanine aminotransferase and/or aspartate aminotransferase reaching 2 times or more of the upper limit of normal value; 3. Patients with acute gout; 4. Patients with unstable angina pectoris, or cardiac insufficiency grade III-IV (NYHA grade), or cerebrovascular diseases such as active intracerebral hemorrhage or new cerebral infarction, or those who need long-term diuretic treatment for any reason; 5. Have serious heart, lung, central nervous system diseases or malignant tumors; 6. Pregnant, pregnant or lactating women; 7. Those who have participated in any drug trial within 3 months before enrollment; 8. Those who cannot sign the informed consent form and do not agree to regular follow-up; 9. Other researchers think it is not suitable to be selected for this experiment.

Design outcomes

Primary

MeasureTime frame
serum creatinine;urine protein;Glomerular filtration rate;24-hour urine biochemistry;Renal B-ultrasound;

Secondary

MeasureTime frame
total CO2;urine pH;blood pH;ALT;AST;Blood electrolyte;blood pressure;Blood bicarbonate;Dual energy CT of kidney;serum uric acid;blood sugar;Blood Fat;

Countries

China

Contacts

Public ContactBao Hui
m13764277007@163.com+86 13764277007

Outcome results

None listed

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