Effect of Hyperuricaemia on Chronic Renal Disease
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|ClinicalTrials.gov Identifier: NCT03425708|
Recruitment Status : Recruiting
First Posted : February 7, 2018
Last Update Posted : February 7, 2018
|Condition or disease||Intervention/treatment||Phase|
|Hyperuricemia Chronic Renal Disease||Drug: 20mg Febuxostat Drug: 40mg Febuxostat||Phase 4|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||400 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Study on the Effect of Hyperuricaemia on Chronic Renal Disease and Intervention|
|Actual Study Start Date :||January 1, 2017|
|Estimated Primary Completion Date :||December 31, 2018|
|Estimated Study Completion Date :||December 31, 2018|
Active Comparator: Treatment group1
Febuxostat pill 20mg was used to treat CKD patients with hyperuricaemia.
Drug: 20mg Febuxostat
Participants take 20mg febuxostat pill once a day for at least six months.
Other Name: 20mg Febuxostat pill group
Active Comparator: Treatment group2
Febuxostat pill 40mg was used to treat CKD patients with hyperuricaemia.
Drug: 40mg Febuxostat
Participants take 40mg febuxostat pill once a day for at least six months.
Other Name: 40mg Febuxostat pill group
No Intervention: Control group
Treatment of CKD patients with hyperuricaemia with conventional methods.
- serum uric acid [ Time Frame: up to 6 months ]intravenous blood sampling
- serum creatinine [ Time Frame: up to 6 months ]intravenous blood sampling
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03425708
|Contact: Dong Sun, MDfirstname.lastname@example.org|
|The Affiliated Hospital of Xuzhou Medical University||Recruiting|
|Xuzhou, Jiangsu, China, 221000|
|Contact: Dong Sun, MD 15862158578 email@example.com|
|Study Director:||Dong Sun, MD||Affiliated Hospital of Xuzhou Medical University|