AzTrials
AzTrials

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.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

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

Other trials in Germany

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.

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 groups in NCT07544797
Study groupRoleWhat they receive
Pea fibreExperimentalParticipants receive baked goods containing a daily amount of 20g inner pea fibres
Receives: Dietary Supplement: praebiotic inner fermentable pea fibres
ControlPlacebo comparatorParticipants 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.

  1. Indoxylsulfate plasma concentration

    µg/ml

    Measured: 8 weeks

Secondary outcomes (9)
  1. p-cresyl sulfate plasma concentration

    µg/ml

    Measured: 8 weeks

  2. Trimethylamin-N-oxide plasma concentration

    µmol/l

    Measured: 8 weeks

  3. Tumor necrosis factor alpha plasma concentration

    pg/ml

    Measured: 8 weeks

  4. Interleukin-6 plasma concentration

    pg/ml

    Measured: 8 weeks

  5. C-reactive protein plasma concentration

    mg/l

    Measured: 8 weeks

  6. Fibroblast growth factor 23 plasma concentration

    pg/ml

    Measured: 8 weeks

  7. Total plasma cholesterol concentration

    mmol/l

    Measured: 8 weeks

  8. LDL cholesterol plasma concentration

    mmol/l

    Measured: 8 weeks

  9. 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.

  1. First posted22 Apr 2026
  2. Study start1 May 2026 (estimated)
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

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)
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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in