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Effects of probiotics and prebiotics on protein-bound uremic toxins and intestinal microflora in peritoneal dialysis patients

Effects of probiotics and prebiotics on protein-bound uremic toxins and intestinal microflora in peritoneal dialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087407
Enrollment
Unknown
Registered
2024-07-26
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

end-stage renal disease

Interventions

Control group:Placebo
Probiotics group:Probiotics(Bifidobacterium longum CCFM1195)
Prebiotics group:Fructooligosaccharides
Yam polysaccharides
Probiotics+Prebiotics group:(Bifidobacterium longum CCFM1195+Fructooligosaccharides
Bergamot)

Sponsors

the Affiliated Wuxi People's Hospital to Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Meet KDIGO criteria for diagnosis and staging of chronic kidney disease 2.Duration of continuous ambulatory peritoneal dialysis treatment =3 months 3.Age 18-75 years old, gender unlimited 4.Willing to participate with full and informed consent

Exclusion criteria

Exclusion criteria: 1. Patients who have taken antibiotics, glucocorticoids or other immunosuppressants, foods and drugs containing probiotics and prebiotics within the past 2 months; 2. Patients with unstable vital signs and condition; 3. Patients who Complicated with active malignant tumor, infection, cardiovascular and cerebrovascular events in the past 3 months; 4. Patients with a history of gastrointestinal bleeding, irritable bowel syndrome, Crohn's disease or ulcerative colitis, or a history of gastrointestinal surgery; 5. Patients with severe malnutrition: Subjective Overall Assessment (SGA) > 15; Anemia Hb< 90g/L 6. Pregnant or lactating women; 7. Patients are unable, unwilling, or do not agree to comply with study requirements, including lifestyle adjustments, follow-up visits, and subject duties; 8. Patients with a history of kidney transplantation or who plan to receive kidney transplantation within 6 months; 9. Patients are allergic or intolerant to the ingredients of the experimental probiotic products; 10.Patients are in other clinical trials.

Design outcomes

Primary

MeasureTime frame
protein-bound uremic toxins ;intestinal microflora ;SF - 36 scale;

Secondary

MeasureTime frame
blood routine;blood biochemistry;inflammatory marks;SGA score;

Countries

China

Contacts

Public ContactWang liang

The Affiliated Wuxi People's Hospital to Nanjing Medical University

wangliang_wuxi@126.com+86 137 7101 9880

Outcome results

None listed

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