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Investigation of probiotic effect on Patients with Chronic Kidney Disease

Investigation of Multi-Strain Synbiotic effect on Kidney Function and quality of life in Patients with Chronic Kidney Disease (CKD)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250629066289N1
Enrollment
88
Registered
2025-09-15
Start date
2025-09-06
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

chronic kidney disease. Chronic kidney disease (CKD)

Interventions

Intervention 1: Intervention group: One synbiotic capsule will be administered daily for 12 weeks, containing the following probiotics: Lactobacillus casei, Lactobacillus rhamnosus, Lactobacillus acid

Sponsors

Yasouj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 60 chronic kidney disease (CKD) - GFR between 30 and 60 (Stage 3 and 4 CKD) - Not receiving renal replacement therapy

Exclusion criteria

Exclusion criteria: _Current Probiotic Use in Specific Populations - Pregnant women - Kidney transplant patients - Patients with gastrointestinal disorders (dysphagia, gastrectomy, irritable bowel syndrome) - Patients with active cancer - Individuals with psychiatric disorders undergoing treatment - Paralyzed or bedridden individuals - Patients with HIV/AIDS, tumors, or autoimmune diseases - Patients receiving treatment with antibiotics, NSAIDs, or corticosteroids

Design outcomes

Primary

MeasureTime frame
Glomerular Filtration Rate. Timepoint: At baseline and at 12 weeks post-intervention. Method of measurement: CKD-EPI.;Quality of life. Timepoint: At baseline and at 12 weeks post-intervention. Method of measurement: Kidney disease quality of life; KDQOL-SFTM 1.3.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamad Kheirkhah

Yasouj University of Medical Sciences

samadkheirkhah65@gmail.com+98 74 3322 0166

Outcome results

None listed

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