Under the premise of double-blind and non-interference clinical treatment, to evaluate the clinical efficacy and safety of probiotic Lactobacillus Zhang combined with routine treatment for gout hyperuricemia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
300
Patients will be randomly assigned to the routine treatment + placebo group and probiotics + routine treatment group according to 1:2 ratio.
Patients will be randomly assigned to the routine treatment + placebo group and probiotics + routine treatment group according to 1:2 ratio.
Inner Mongolia Medical College Affiliated Hospital
Hohhot, Inner Mongolia, China
RECRUITINGserum uric acid level
The serum uric acid level was standard-reaching rate at the end of 24 weeks(Percentage of patients whose serum uric acid level has decreased to less than 360umol / L )
Time frame: 24 weeks
serum uric acid level at the 4、8、12、24 weeks
the serum uric acid level and the percentage of patients with \< 360umol / L at the end of 4, 8, 12 and 24 weeks after treatment
Time frame: 4、8、12、24 weeks
serum uric acid decreased from baseline
At the end of 4, 8, 12 and 24 weeks after treatment, the serum uric acid level decreased from baseline
Time frame: 4、8、12、24 weeks
Acute attack of gout
Number of acute gout attacks during 24 weeks of treatment
Time frame: 24 week
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