HemodialysisMUFINNCT07544797
Pea Fibre in Hemodialysis
A study testing praebiotic inner fermentable pea fibres in people with Hemodialysis and Kidney Failure Chronic, run by Martin-Luther-Universität Halle-Wittenberg at 1 site in Germany.
Trial summary
Background and problem Chronic kidney disease (CKD) affects a large share of adults worldwide and is a growing public-health concern. People with advanced CKD can develop "uremia", a dangerous build-up of waste products in the blood that the failing kidneys cannot remove. Read more about this study
- Who is it for?
- Ages 18 to 89 years
- Conditions the study is for
- Hemodialysis, Kidney Failure Chronic
- What is being tested?
- praebiotic inner fermentable pea fibres
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 72 participants
- Where
- 1 siteGermany
- Study dates
- 1 May 2026to 31 Dec 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 89 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- male and female patients 18-89 years of age
- chronic hemodialysis treatment minimum 3 months for any kind of kidney disease
- 2-3 hemodialysis sessions per week
- expected to continue regular treatment for at least 3 months
- written informed consent
Who cannot join
- Persons younger than 18 or older than 89 years
- Clinically relevant infections at the time of the study or within 2 weeks prior to study inclusion
- Use of immunosuppressive medications, with the exception of glucocorticoids ≤ 5 mg prednisolone equivalent
- Liver cirrhosis, Child-Pugh stage C
- Active malignancy, with or without specific oncological therapy
- Blood transfusion within 4 weeks prior to inclusion, or severe anemia with a current indication for blood transfusion
Show all 13Show fewer
- Planned absence (e.g., vacation) for more than 1 week during the study period
- Pregnancy
- Intolerance to gluten, eggs, milk, yeast, nuts, or pea protein
- Missing consent to participate in the study
- Inability to understand the study content and procedures and to provide informed consent after appropriate explanation
- Persons institutionalized by court or administrative order
- Simultaneous participation in another interventional study
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Germany1 site
University Hospital Martin-Luther-University Halle-Wittenberg
Halle, Saxony-Anhalt, D06120
Matthias Girndt, MD, +49 345 557 2717, matthias.girndt@uk-halle.de
Roman Fiedler, MD, +49 345 582 970, roman.fiedler@uk-halle.de
About this study
Official title: Influencing Microbiota and Uremic Toxins With Pea Fibre Intervention in Nephrology
Background and problem Chronic kidney disease (CKD) affects a large share of adults worldwide and is a growing public-health concern. People with advanced CKD can develop "uremia", a dangerous build-up of waste products in the blood that the failing kidneys cannot remove. Even when patients receive regular dialysis, many so-called "uremic toxins" remain in the body because some of these substances bind tightly to blood proteins and are poorly removed by dialysis. Over 100 uremic toxins have been identified and classified and protein-bound toxins such as Indoxylsulfate and p-Cresylsulfate are especially difficult to clear by dialysis.
Some uremic toxins are linked to heart and blood-vessel disease, inflammation, and worse outcomes in dialysis patients. For example, Indoxylsulfate has been associated with higher mortality, vascular calcification, vessel stiffness and heart failure. Reducing these toxins might therefore improve quality of life and lower cardiovascular risk in people on dialysis.
Read more
Purpose of the study The study will test whether adding inner, fermentable pea fiber (a natural prebiotic) to the daily diet of hemodialysis patients can lower blood levels of uremic toxins-especially Indoxylsulfate-and improve related markers of inflammation and cardiovascular risk. The investigators hypothesize that fermentable fibers change gut bacterial composition so that less toxin-forming bacterial metabolism (from amino acids like tryptophan) occurs, thereby reducing the amount of harmful metabolites that reach the blood.
Type of study: Randomized, double-blind, controlled trial with two groups. Duration: 8 weeks of intervention. Intervention: Participants will receive daily baked goods (bread, rolls, muffins, scones, pizza bread) that together provide 20 g of pea fiber per day; the control group will receive identical foods without added pea fiber. The fiber mix uses commercially available inner pea-fiber products.
Blood and stool sampling: Blood samples are taken before the intervention, at 4 weeks and at 8 weeks to measure Indoxylsulfate and other toxins, inflammation markers, vitamin D metabolites and cardiovascular risk markers. A subgroup will also provide stool samples to study changes in the gut microbiome.
Who can join Adults aged 18-89 who have been on chronic hemodialysis for at least three months and receive dialysis two to three times per week are eligible. The study excludes people with recent serious infections, advanced liver disease, active cancer, recent blood transfusion, pregnancy, certain food intolerances or inability to consent. Each study arm will include 36 participants.
Primary and secondary outcomes Primary outcome: Change in blood Indoxylsulfate concentration between the pea-fiber group and the control group.
Secondary outcomes: Levels of other uremic toxins, routine kidney-related blood tests (creatinine, urea, uric acid), electrolytes, vitamin D metabolites, inflammatory markers, lipid markers, FGF23, short-chain fatty acids, sKlotho, and the effect of patient serum on cytokine production in a standard immune cell line. Stool analyses in a subgroup will examine shifts in bacterial groups and metabolic networks.
How the intervention is delivered and monitored Foods are prepared in a certified bakery and coded so neither participants nor study staff know who receives pea fiber or placebo. To improve adherence, participants choose from a variety of pre-portioned baked items and are advised to spread intake across the day. Unused portions are returned and logged. Dietary recalls and symptom questionnaires are collected to monitor changes in overall diet, appetite and gastrointestinal side effects. Blood draws are timed before dialysis after the long interdialytic interval to standardize measurements.
Potential impact and limitations If fermentable inner pea fibers lower Indoxylsulfate and related toxins, this would support a simple, food-based strategy to reduce toxin burden and possibly cardiovascular risk in dialysis patients. However, previous studies show mixed results depending on the type of fiber used: fermentable fibers (like amylose-rich starch or inulin) have produced beneficial changes in some trials, while non-fermentable fibers did not. Since evidence high-quality randomized trials in dialysis patients is still limited there is the need for this study.
- Conditions
- Hemodialysis, Kidney Failure Chronic
- Being tested
- praebiotic inner fermentable pea fibres, Control
- Keywords
- prebiotics, hemodialysis, pea fibre, indoxylsulfate, kidney failure chronic, uremic toxin
- Medical subject headings
- Renal Insufficiency, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
praebiotic inner fermentable pea fibresDietary supplement
prebiotic pea fibres baked into bread, rolls, muffins, scones or pizza bread in the intervention group.
ControlDietary supplement
Similar baked goods without prebiotic ingredients.
| Study group | Role | What they receive |
|---|---|---|
| Pea fibre | Experimental | Participants receive baked goods containing a daily amount of 20g inner pea fibres Receives: Dietary Supplement: praebiotic inner fermentable pea fibres |
| Control | Placebo comparator | Participants receive identical baked good without inner pea fibres Receives: Dietary Supplement: Control |
What is being measured
The primary outcome is the main question the study is designed to answer.
Indoxylsulfate plasma concentration
µg/ml
Measured: 8 weeks
Secondary outcomes (9)
p-cresyl sulfate plasma concentration
µg/ml
Measured: 8 weeks
Trimethylamin-N-oxide plasma concentration
µmol/l
Measured: 8 weeks
Tumor necrosis factor alpha plasma concentration
pg/ml
Measured: 8 weeks
Interleukin-6 plasma concentration
pg/ml
Measured: 8 weeks
C-reactive protein plasma concentration
mg/l
Measured: 8 weeks
Fibroblast growth factor 23 plasma concentration
pg/ml
Measured: 8 weeks
Total plasma cholesterol concentration
mmol/l
Measured: 8 weeks
LDL cholesterol plasma concentration
mmol/l
Measured: 8 weeks
Triglyceride plasma concentration
mmol/l
Measured: 8 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Apr 2026
- Study start1 May 2026 (estimated)
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HemodialysisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 72 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Martin-Luther-Universität Halle-Wittenberg
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Matthias Girndt, Martin-Luther-Universität Halle-Wittenberg
- Investigators
- Matthias Girndt, MD, Study director, Martin-Luther-University Halle-Wittenberg
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07544797
- Sponsor's protocol ID
- UKH-KIMII-001-26
- Acronym
- MUFIN
- Status last verified
- Apr 2026
- First submitted
- 8 Apr 2026
- Last updated
- 22 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Influencing Microbiota and Uremic Toxins With Pea Fibre Intervention in Nephrology
- ClinicalTrials.gov ID
- NCT07544797
- Acronym / sponsor ID
- MUFIN / UKH-KIMII-001-26
- Conditions
- Hemodialysis, Kidney Failure Chronic
- Keywords
- prebiotics, hemodialysis, pea fibre, indoxylsulfate, kidney failure chronic, uremic toxin
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 72 participants (estimated)
- Lead sponsor
- Martin-Luther-Universität Halle-WittenbergUniversity, hospital or other
- Study start
- 1 May 2026 (estimated)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Dec 2028 (estimated)
- First posted
- 22 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background and problem Chronic kidney disease (CKD) affects a large share of adults worldwide and is a growing public-health concern. People with advanced CKD can develop "uremia", a dangerous build-up of waste products in the blood that the failing kidneys cannot remove. Even when patients receive regular dialysis, many so-called "uremic toxins" remain in the body because some of these substances bind tightly to blood proteins and are poorly removed by dialysis. Over 100 uremic toxins have been identified and classified and protein-bound toxins such as Indoxylsulfate and p-Cresylsulfate are especially difficult to clear by dialysis.
Some uremic toxins are linked to heart and blood-vessel disease, inflammation, and worse outcomes in dialysis patients. For example, Indoxylsulfate has been associated with higher mortality, vascular calcification, vessel stiffness and heart failure. Reducing these toxins might therefore improve quality of life and lower cardiovascular risk in people on dialysis.
Purpose of the study The study will test whether adding inner, fermentable pea fiber (a natural prebiotic) to the daily diet of hemodialysis patients can lower blood levels of uremic toxins-especially Indoxylsulfate-and improve related markers of inflammation and cardiovascular risk. The investigators hypothesize that fermentable fibers change gut bacterial composition so that less toxin-forming bacterial metabolism (from amino acids like tryptophan) occurs, thereby reducing the amount of harmful metabolites that reach the blood.
Type of study: Randomized, double-blind, controlled trial with two groups. Duration: 8 weeks of intervention. Intervention: Participants will receive daily baked goods (bread, rolls, muffins, scones, pizza bread) that together provide 20 g of pea fiber per day; the control group will receive identical foods without added pea fiber. The fiber mix uses commercially available inner pea-fiber products.
Blood and stool sampling: Blood samples are taken before the intervention, at 4 weeks and at 8 weeks to measure Indoxylsulfate and other toxins, inflammation markers, vitamin D metabolites and cardiovascular risk markers. A subgroup will also provide stool samples to study changes in the gut microbiome.
Who can join Adults aged 18-89 who have been on chronic hemodialysis for at least three months and receive dialysis two to three times per week are eligible. The study excludes people with recent serious infections, advanced liver disease, active cancer, recent blood transfusion, pregnancy, certain food intolerances or inability to consent. Each study arm will include 36 participants.
Primary and secondary outcomes Primary outcome: Change in blood Indoxylsulfate concentration between the pea-fiber group and the control group.
Secondary outcomes: Levels of other uremic toxins, routine kidney-related blood tests (creatinine, urea, uric acid), electrolytes, vitamin D metabolites, inflammatory markers, lipid markers, FGF23, short-chain fatty acids, sKlotho, and the effect of patient serum on cytokine production in a standard immune cell line. Stool analyses in a subgroup will examine shifts in bacterial groups and metabolic networks.
How the intervention is delivered and monitored Foods are prepared in a certified bakery and coded so neither participants nor study staff know who receives pea fiber or placebo. To improve adherence, participants choose from a variety of pre-portioned baked items and are advised to spread intake across the day. Unused portions are returned and logged. Dietary recalls and symptom questionnaires are collected to monitor changes in overall diet, appetite and gastrointestinal side effects. Blood draws are timed before dialysis after the long interdialytic interval to standardize measurements.
Potential impact and limitations If fermentable inner pea fibers lower Indoxylsulfate and related toxins, this would support a simple, food-based strategy to reduce toxin burden and possibly cardiovascular risk in dialysis patients. However, previous studies show mixed results depending on the type of fiber used: fermentable fibers (like amylose-rich starch or inulin) have produced beneficial changes in some trials, while non-fermentable fibers did not. Since evidence high-quality randomized trials in dialysis patients is still limited there is the need for this study.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Pea fibre | Experimental | Dietary Supplement: praebiotic inner fermentable pea fibresParticipants receive baked goods containing a daily amount of 20g inner pea fibres |
| Control | Placebo comparator | Dietary Supplement: ControlParticipants receive identical baked good without inner pea fibres |
Who may qualify
- Ages
- 18 to 89 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- male and female patients 18-89 years of age
- chronic hemodialysis treatment minimum 3 months for any kind of kidney disease
- 2-3 hemodialysis sessions per week
- expected to continue regular treatment for at least 3 months
- written informed consent
Key exclusion criteria (13 listed)
- Persons younger than 18 or older than 89 years
- Clinically relevant infections at the time of the study or within 2 weeks prior to study inclusion
- Use of immunosuppressive medications, with the exception of glucocorticoids ≤ 5 mg prednisolone equivalent
- Liver cirrhosis, Child-Pugh stage C
- Active malignancy, with or without specific oncological therapy
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| praebiotic inner fermentable pea fibresprebiotic pea fibres baked into bread, rolls, muffins, scones or pizza bread in the intervention group. | Dietary supplement | Pea fibre |
| ControlSimilar baked goods without prebiotic ingredients. | Dietary supplement | Control |
Primary outcome
Indoxylsulfate plasma concentration
Time frame: 8 weeks
µg/ml
9 secondary outcomes
p-cresyl sulfate plasma concentration
Time frame: 8 weeks
Trimethylamin-N-oxide plasma concentration
Time frame: 8 weeks
Tumor necrosis factor alpha plasma concentration
Time frame: 8 weeks
Interleukin-6 plasma concentration
Time frame: 8 weeks
C-reactive protein plasma concentration
Time frame: 8 weeks
Fibroblast growth factor 23 plasma concentration
Time frame: 8 weeks
Total plasma cholesterol concentration
Time frame: 8 weeks
LDL cholesterol plasma concentration
Time frame: 8 weeks
Triglyceride plasma concentration
Time frame: 8 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Apr 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Matthias Girndt, MD study director
Martin-Luther-University Halle-Wittenberg
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing praebiotic inner fermentable pea fibres in people with Hemodialysis and Kidney Failure Chronic, run by Martin-Luther-Universität Halle-Wittenberg at 1 site in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 22 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Matthias Girndt, MD (+49 345 557 2717, matthias.girndt@uk-halle.de), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Indoxylsulfate plasma concentration (time frame: 8 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2026.