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Effects of probiotic Lactobacillus rhamnosus CCFM1130, Lactobacillus reuteri CCFM1132 and Lactobacillus gasseri CCFM1133 on relieving hyperuricemia and regulating gut microbiota

Effects of probiotic Lactobacillus rhamnosus CCFM1130, Lactobacillus reuteri CCFM1132 and Lactobacillus gasseri CCFM1133 on relieving hyperuricemia and regulating gut microbiota

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072246
Enrollment
Unknown
Registered
2023-06-07
Start date
2023-06-15
Completion date
Unknown
Last updated
2023-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperuricemia

Interventions

Lactobacillus rhamnosus CCFM1130:Lactobacillus rhamnosus CCFM1130
Lactobacillus reuteri CCFM1132:Lactobacillus reuteri CCFM1132
Lactobacillus gasseri CCFM1133 :Lactobacillus gasseri CCFM1133
placebo:placebo

Sponsors

Yixing People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) He/She meets the diagnostic criteria of hyperuricemia; (2) 18 years = age = 65 years, male or female; (3) The blood uric acid level was detected twice on an empty stomach on different days, which was higher than 420 in men µ Mol/L, higher than 360 for women µ mol/L (4) Good compliance, able to comply with the requirements of clinical trials; (5) The subject or guardian has signed the informed consent form; (6) The patients filled in the written informed consent form, the International Physical Activity Scale and the dietary structure questionnaire, and promised to cooperate with the study during the whole trial period.

Exclusion criteria

Exclusion criteria: (1) Equivalent intake of ethanol>40 g/week; (2) Take non-steroidal anti-inflammatory drugs, antibiotics and corticosteroids, anti-tumor drugs, anti-tuberculosis drugs and some Chinese herbal and mineral drugs (Acer truncatum/arsenic trioxide) regularly in the past six months; (3) Abuse of narcotics, psychotropic substances and cigarettes in the past 6 months; (4) Ingestion in the past 6 months caused gastric acid deficiency, amiodarone, sodium valproate, prednisone, tamoxifen, piperacillin and methotrexate, liver fat induction drugs, hormone drugs, statins, antihypertensive drugs and ursodeoxycholic acid anti-secretory drugs. (5) During the study period or in the past 3 months, supplement nutrients at least twice a week, such as probiotics, vitamins/minerals, antioxidants and ?- 3 (6) Patients with acute gout attack (7) Secondary hyperuricemia caused by glomerular disease, lead poisoning, hematological disease, tumor radiotherapy, chemotherapy or long-term use of diuretics. Patients with serious primary diseases and mental diseases such as cardiovascular, cerebrovascular, liver and kidney and hematopoietic system. (8) Patients with long-term or recent use of drugs that affect blood uric acid. (9) In the past 6 months, the body weight has been rapidly reduced, and total parenteral nutrition and protein malnutrition have occurred. (10) Pregnant or lactating women (11) Allergic or intolerant to the ingredients of the probiotic products tested; (12) The patient's compliance is poor and the possibility of follow-up is poor;

Design outcomes

Primary

MeasureTime frame
Fecal flora;Renal routine;Fecal flora genomics;Blood routine;hepatic function;Fecal routine;

Secondary

MeasureTime frame
Height;Weight;

Countries

China

Contacts

Public ContactLiyun Wang

Yixing People's Hospital

staff532@yxph.com+86 139 6151 9301

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026