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COMPLETED
NCT07260292
NA

KPs Supplement for Inflammation, Oxidative Stress and Lipid Abnormalities in CKD Patients.

Sponsor: National Chung Hsing University

View on ClinicalTrials.gov

Summary

This clinical investigation is designed to evaluate the potential therapeutic effects of kefir peptides as an adjunct intervention for chronic kidney disease (CKD) and clinical proteinuria. Patients diagnosed with stage 3 or 4 CKD will receive a three-month course of kefir peptide supplementation. Throughout the intervention period, the investigator will monitor renal function markers (blood urea nitrogen, serum creatinine), proteinuria (urine protein-to-creatinine ratio), inflammatory indicators (high-sensitivity C-reactive protein), and additional biochemical parameters relevant to CKD progression.

Official title: Kefir Peptides Supplement for Inflammation, Oxidative Stress and Lipid Abnormalities in Chronic Kidney Disease Patients

Key Details

Gender

All

Age Range

30 Years - 82 Years

Study Type

INTERVENTIONAL

Enrollment

165

Start Date

2023-02-03

Completion Date

2024-08-02

Last Updated

2026-09-01

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

KEFPEP®

oral administration at a daily dosage of 2.4 grams for 12 weeks

DIETARY_SUPPLEMENT

Placebo

using regular yogurt powder as a substitute for KPs

Locations (1)

Jen-Ai Hospital

Taichung, Taiwan