Clinical Trials Directory

Trials / Completed

CompletedNCT00793585

A Controlled Study of Uric Acid on the Progression of IgA Nephropathy

A Prospective, Randomized Controlled Study of Uric Acid on the Progression of IgA Nephropathy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This prospective, randomized controlled study will evaluate the effect of uric acid on the progression of IgA nephropathy.

Detailed description

It has been reported that hyperuricemia is a risk factor for progression of IgAN. This will be a prospective, randomized study. Eligible IgAN patients will be randomized into the treatment group and the control group. Patients in treatment group will receive allopurinol and usual therapy. Patients in control group will receive usual therapy with placebo. If with hypertension, add the CCB and the β-blocker. Fasting uric acid, serum creatinine, albumin, routine blood test, urine microscopy and dipstick, proteinuria of 24 hours and blood pressure will be measured every month. After followed-up for 6 months, the curative effect of Allopurinol on blood pressure, proteinuria and the progression of IgA nephropathy will be evaluated.

Conditions

Interventions

TypeNameDescription
DRUGallopurinolPatients will receive the lifestyle modification and treatment of allopurinol (300 mg /d) and lifestyle modification for 4 weeks; when the UA level \< 6mg/dl , the dosage changed to 200mg/d.
OTHERcontinue their usual therapyPatients will receive lifestyle modification and continue their usual therapy.

Timeline

Start date
2007-07-01
Primary completion
2009-06-01
Completion
2009-06-01
First posted
2008-11-19
Last updated
2016-05-25
Results posted
2011-07-01

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00793585. Inclusion in this directory is not an endorsement.