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Gut health boost may ease kidney disease inflammation
NCT ID NCT07430280
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a daily synbiotic supplement (probiotics plus prebiotics) can lower inflammation and improve digestive symptoms in adults with chronic kidney disease stages 3 to 5 who are not yet on dialysis. One hundred participants will receive either the supplement or a placebo for 16 weeks. The goal is to see if this simple nutritional approach can help manage inflammation and improve quality of life.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 to 80 years. * Diagnosis of chronic kidney disease in pre-dialysis stages. * Stable clinical condition for at least 3 months prior to enrollment. * Ability to provide written informed consent. Exclusion Criteria: * Current renal replacement therapy (hemodialysis or peritoneal dialysis). * Acute kidney injury. * Use of antibiotics, probiotics, prebiotics, or synbiotics within 4 weeks prior to enrollment. * Active infection, inflammatory disease, or malignancy. * Pregnancy or breastfeeding * Known intolerance or allergy to components of the synbiotic or placebo.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
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