NCT02338323

Brief Summary

The purpose of this study is to determine whether febuxostat and benzbromarone could protect renal function, and which one could be better.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2015

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2015

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

January 10, 2015

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 14, 2015

Completed
3.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2018

Completed
Last Updated

July 24, 2019

Status Verified

July 1, 2019

Enrollment Period

3.9 years

First QC Date

January 10, 2015

Last Update Submit

July 23, 2019

Conditions

Keywords

HyperuricemiaRenal FunctionChronic kidney diseaseFebuxostatBenzbromarone

Outcome Measures

Primary Outcomes (1)

  • Renal function

    Blood test for serum uric acid and creatinine, according to equation to estimate glomerular filtration rate

    up to 12th months

Secondary Outcomes (2)

  • urine protein

    3rd months, 6th months, 9th months, 12th months

  • adverse drug reaction

    1st month, 2nd months, 3rd months, 6th months, 9th months, 12th months

Study Arms (2)

Febuxostat

EXPERIMENTAL

take orally, 40mg per day, for 1 year

Drug: Febuxostat

Benzbromarone

EXPERIMENTAL

take orally, 50mg per day, for 1 year

Drug: Benzbromarone

Interventions

It acts as an inhibitor of xanthine oxidase, thus lowering urate concentrations in the body

Also known as: Uloric, Adenuric
Febuxostat

It is structurally related to the antiarrhythmic amiodarone, and it is a uricosuric agent and non-competitive inhibitor of xanthine oxidase

Also known as: Desuric
Benzbromarone

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Chronic kidney disease patients with glomerular filtration rate (GFR,20-50ml/min) who match one of the following criteria:
  • Gout
  • Hyperuricemia patients without gout but have cardiovascular risk and serum uric acid \> 480umol/L
  • Hyperuricemia patients without gout but with serum uric acid \> 540umol/L

You may not qualify if:

  • GFR\<20ml/min or GFR \>50ml/min
  • Liver dysfunction (Aspartate transaminase or/and alanine aminotransferase exceed 2 times of normal range)
  • Urinary tract obstruction
  • unstable angina, heart failure (stage III-IV, NYHA), new stroke, need diuretics for long-term treatment
  • Severe lung diseases or cancers
  • Pregnant woman or woman who prepare to be pregnant,nursing mothers
  • unable to sign informed consent form,or disagree with following-up

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Nephrology & Rheumatology, Shanghai Tenth People's Hospital

Shanghai, Shanghai Municipality, 200072, China

Location

MeSH Terms

Conditions

Renal Insufficiency, ChronicHyperuricemia

Interventions

FebuxostatBenzbromarone

Condition Hierarchy (Ancestors)

Renal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

ThiazolesSulfur CompoundsOrganic ChemicalsAzolesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsBenzofuransHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Study Officials

  • Ling Wang, MD, PhD

    Department of Nephrology & Rheumatology, Shanghai Tenth People's Hospital

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief of department of Nephrology & Rheumatology

Study Record Dates

First Submitted

January 10, 2015

First Posted

January 14, 2015

Study Start

January 1, 2015

Primary Completion

December 1, 2018

Study Completion

December 1, 2018

Last Updated

July 24, 2019

Record last verified: 2019-07

Locations