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Effects of probiotics on uremic toxins and intestinal microflora in patients with chronic kidney disease

Effects of probiotics on uremic toxins and intestinal microflora in patients with chronic kidney disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013952
Enrollment
Unknown
Registered
2017-12-15
Start date
2018-07-09
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

Chronic kidney disease

Interventions

placebo group:Oral placebo
probiotic group:Oral L. casei Zhang

Sponsors

Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Aged 18-75 years old; 2.In line with KDIGO diagnosis of chronic kidney disease staging standards; 3.CKD stage 3-5, did not receive dialysis treatment, no dialysis indications, temporary stable condition, the drug can control the stage; 4.To be informed and volunteer to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating; 2. Female patients who did not use any contraception; 3. Vital signs unstable, unstable patients; 4. There are difficult to correct hyperkalemia, heart failure and other indicators of dialysis emergency dialysis; 5. After uncontrolled by conservative medical treatment, one of the following conditions is still excluded: Hb <70g / L; or carbon dioxide binding strength <13mmol / L; 6. With active malignancy, stroke, myocardial infarction and other serious primary diseases; 7. Have gastrointestinal bleeding, irritable bowel syndrome, Crohn's disease or ulcerative colitis and other gastrointestinal diseases, history of gastrointestinal surgery patients with history; 8. Patients with a history of mental illness; 9. There is a history of renal transplantation or kidney transplantation within 6 months; 10 in the past 1 month to take antibiotics, glucocorticoids or other immunosuppressive agents, including probiotics, prebiotics of food, medicine and other patients; 11. The test sample allergy or obvious gastrointestinal symptoms such as those who can not tolerate; 12. Patients who receive other clinical trials at the same time; 13. The researcher can not confirm the completion of the researcher on time.

Design outcomes

Primary

MeasureTime frame
Creatinine;Indoxyl sulfate;P-cresyl sulfate;

Countries

China

Contacts

Public ContactYing Yao

Tongji Hospital

yaoyingkk@126.com+86 13720379867

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026