a statement of the study hypothesis:the effect of valsartan in patients with IgA nephropathy have been proved,and the efficacy of probucol in combination with valsartan is to be proved in patients with IgA nephropathy. This is a prospective randomized controlled, double blinded pilot study to identify the efficacy of probucol in combination with valsartan in patients with IgA nephropathy. The renal function deterioration will be the primary outcome studied. The expected study duration will be 36 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
75
Valsartan (80-160mg/day)
Probucol (750mg/day)
Placebo
Guangdong General Hospital
Guangzhou, Guangdong, China
urinary protein loss whithin 24 hours
Time frame: 2-3years
renal function(serum Crea or eGFR) deterioration
Time frame: 2-3years
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