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Effect of Hyperuricaemia on Chronic Renal Disease

X

Xuzhou Medical University

Status and phase

Unknown
Phase 4

Conditions

Chronic Renal Disease
Hyperuricemia

Treatments

Drug: 40mg Febuxostat
Drug: 20mg Febuxostat

Study type

Interventional

Funder types

Other

Identifiers

NCT03425708
XYFY2017-KL043-01

Details and patient eligibility

About

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

Full 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

Enrollment

400 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

400 participants in 3 patient groups

Treatment group1
Active Comparator group
Description:
Febuxostat pill 20mg was used to treat CKD patients with hyperuricaemia.
Treatment:
Drug: 20mg Febuxostat
Treatment group2
Active Comparator group
Description:
Febuxostat pill 40mg was used to treat CKD patients with hyperuricaemia.
Treatment:
Drug: 40mg Febuxostat
Control group
No Intervention group
Description:
Treatment of CKD patients with hyperuricaemia with conventional methods.

Trial contacts and locations

1

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Central trial contact

Dong Sun, MD

Data sourced from clinicaltrials.gov

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