Compare the Renal Protective Effects of Febuxostat and Benzbromarone
1 other identifier
interventional
160
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2015
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2015
CompletedFirst Submitted
Initial submission to the registry
January 10, 2015
CompletedFirst Posted
Study publicly available on registry
January 14, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2018
CompletedJuly 24, 2019
July 1, 2019
3.9 years
January 10, 2015
July 23, 2019
Conditions
Keywords
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
EXPERIMENTALtake orally, 40mg per day, for 1 year
Benzbromarone
EXPERIMENTALtake orally, 50mg per day, for 1 year
Interventions
It acts as an inhibitor of xanthine oxidase, thus lowering urate concentrations in the body
It is structurally related to the antiarrhythmic amiodarone, and it is a uricosuric agent and non-competitive inhibitor of xanthine oxidase
Eligibility Criteria
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
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Ling Wang, MD, PhD
Department of Nephrology & Rheumatology, Shanghai Tenth People's Hospital
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