Skip to content

Effect of Hyperuricaemia on Chronic Renal Disease

Study on the Effect of Hyperuricaemia on Chronic Renal Disease and Intervention

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03425708
Enrollment
400
Registered
2018-02-07
Start date
2017-01-01
Completion date
2018-12-31
Last updated
2018-02-07

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

Conditions

Chronic Renal Disease, Hyperuricemia

Keywords

Uric Acid, Febuxostat, Chronic Renal Disease

Brief summary

To investigate the Effect of Hyperuricaemia on Chronic Renal Disease and Intervention

Detailed description

This study aims to explore the best effective dose and adverse reaction of febuxostat in lowering serum uric acid to low level in patients with Chronic Renal Disease at different stages. To elucidate that low levels of serum uric acid can delay the progression of renal damage. Promote the application of anti uric acid drugs in the treatment of chronic renal failure and delay the progress of CKD in patients

Interventions

DRUG20mg Febuxostat

Participants take 20mg febuxostat pill once a day for at least six months.

DRUG40mg Febuxostat

Participants take 40mg febuxostat pill once a day for at least six months.

Sponsors

The First People's Hospital of Xuzhou
CollaboratorOTHER
The Affiliated Hospital of Xuzhou Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Non-dialysis CKD patients with serum uric acid greater than 7mg/dl. * eGFR≥15ml/min/1.73m². * Low salt, low protein, low purine diet.

Exclusion criteria

* Take drugs that raise blood uric acid at the same time. * Patients with gout attacks. * Patients with pregnant, lactating. * Autosomal dominant polycystic kidney disease. * Patients with poor general condition and multiple organ failure.

Design outcomes

Primary

MeasureTime frameDescription
serum uric acidup to 6 monthsintravenous blood sampling

Secondary

MeasureTime frameDescription
serum creatinineup to 6 monthsintravenous blood sampling

Countries

China

Contacts

Primary ContactDong Sun, MD
sundong126@yahoo.com15862158578

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026