Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
NCT04819217

Study of Oral Uremic Toxin Absorbent and Probiotics to Retard the Progression of Chronic Kidney Disease

Led by National Taiwan University Hospital · Updated on 2025-07-18

180

Participants Needed

1

Research Sites

552 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In patients with chronic kidney disease (CKD), uremic toxins accumulate when kidney function declines. Those uremic toxins had a greater affinity to circulating proteins are called "protein bound uremic toxins, PBUT." Apart from traditional small or middle molecule uremic toxins, the PBUTs can be rarely eliminated using traditional renal replacement therapy, even using high flux dialysis modalities. Among these molecules identified, indoxyl sulfate (IS), and p-cresol (PC) are mostly studied. Both in vitro and in vivo study, IS and PC are associated with endothelial dysfunction, vascular smooth muscle proliferation, and increased risk for CV outcomes. The uremic toxins (IS and PC) are originated in the endogenous environment, mainly from the protein metabolism, food intake, or produced by gut microbiota. Prevention of IS or PC precursors from being absorbed across the intestinal tract has been extensively studied in the renal literature by use of oral adsorbents. In animal models, activated charcoal reduces the serum concentration of creatinine (cre) and may delay CKD progression by alleviating IS overload. An oral form of non-absorbable surface-modified activated bamboo charcoal (ABC), has been demonstrated to effectively reduce circulating and renal IS levels in animal models. Recently, probiotics, prebiotics or synbiotics have been reported to reduce inflammation, improve kidney function and retard progression of CKD by restoring the symbiosis of gut microflora in patients with CKD. A randomized trial found synbiotics decreased serum PCS without reducing serum IS in non-dialysis CKD. Another study found that synbiotics delayed CKD progression. A systematic review found prebiotic and probiotic therapies reduced IS and PCS in patients with end stage kidney disease (ESKD) on haemodialysis. However, it is unclear whether the results hold true for other patients with CKD. Based on these previous findings, investigators will conduct a prospective randomized open blinded end-point (PROBE) study to see if oral uremic toxin absorbent + probiotics prevent CKD progression. Also, a panel of clinical and biochemical profiles will be checked to investigate possible link between several biomarkers and clinical response.

CONDITIONS

Official Title

Study of Oral Uremic Toxin Absorbent and Probiotics to Retard the Progression of Chronic Kidney Disease

Who Can Participate

Age: 20Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 20 years or older on the day of screening
  • Diagnosed with chronic kidney disease having eGFR between 15 and 45 ml/min/1.73m2
  • Urine albumin to creatinine ratio (UACR) greater than 100 mg/g
  • Stable kidney function with creatinine increase less than 0.3 mg/dL in the 30 days before enrollment
Not Eligible

You will not qualify if you...

  • Estimated glomerular filtration rate (eGFR) less than 15 ml/min/1.73m2
  • Severe malnutrition with albumin less than 2.0 g/dL
  • Severe anemia or active gastrointestinal bleeding with hemoglobin less than 8 g/dL
  • Peptic ulcer, esophageal varices, ileus, or currently fasting
  • Previous gastrointestinal surgery
  • Chronic constipation with fewer than 3 bowel movements per week unless controlled by laxatives
  • History of major hemorrhage requiring blood transfusion during recent hospital admission
  • Advanced liver cirrhosis classified as Child B or C
  • History of solid organ or blood cell transplantation
  • Oliguric kidney injury with urine output less than 500 cc/day
  • Obstructive kidney injury or polycystic kidney disease
  • Use of antibiotics or probiotics within 2 weeks before enrollment or during the study
  • History or presence of cancer within the past 5 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

NTUH

Taipei, Taiwan

Actively Recruiting

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Research Team

C

Chau chung Wu, Ph.D.

CONTACT

M

Mei-Chang Huang, Master

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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