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Clinical Trial Summary

The purpose of this Phase 1, 3-period crossover with repeated measures feasibility study is to characterize the gut microbiome of individuals with chronic kidney disease, and to explore effects of p-inulin on the gut microbiome. The nature of the study will provide information about the feasibility of stool sample collection for future multicenter studies of the gut microbiome.


Clinical Trial Description

The overarching hypothesis motivating this exploratory study of variability is that treatment with oligofructose-enriched inulin (p-inulin) will alter the composition and/or function of the gut microbiome, and thereby reduce the generation of gut-derived uremic toxins, improve gut barrier function and attenuate systemic inflammation in CKD patients. In order to design a future clinical trial the following parameters from CKD subjects are needed:

1. Intra-patient variability in the composition and function of the gut microbiome

2. Inter-patient variability in the composition and function of the gut microbiome

3. Impact of p-inulin on the composition and function of the gut microbiome

4. Tolerability of p-inulin administration

5. Feasibility of collecting stool samples in this patient population ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03348592
Study type Interventional
Source National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Contact
Status Active, not recruiting
Phase N/A
Start date October 2016
Completion date June 2018

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