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Tolerance of Regular Meal Intake With Mycoprotein (TOMMY)

Tolerance of Regular Meal Intake With Mycoprotein

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04590768
Enrollment
24
Registered
2020-10-19
Start date
2020-10-12
Completion date
2020-11-02
Last updated
2021-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal Complication

Keywords

Fermotein™, Gastrointestinal tolerance

Brief summary

This study aims to assess the impact of daily intake of 11 grams of Fermotein™ on gastrointestinal complaints and several other health related biomarkers. Furthermore, consumer acceptance is investigated. The study has a randomized parallel design. Two different treatments will be evaluated e.g. a 18-day intervention with fermotein based meals and a 18-day intervention with control meals. At the start and at the end of the intervention, a blood sample will be collected. Questionnaires about gut complaints, stool consistency and frequency, wellbeing, health complaints or other adverse effects will be collected daily during intervention and up to two days after the intervention.

Detailed description

Fermotein™ is a mycoprotein, derived from fungi, especially produced for human consumption. It is high in protein, high in fiber, low in saturated fat and contains no cholesterol. Its functional properties and nutrient content makes them ideal to use as an ingredient for meat alternatives and other vegetarian/vegan food products. This study aims to assess the impact of frequent intake of 11 grams of Fermotein™ powder (dry) on gastrointestinal complaints and several other health related biomarkers. The primary objective is to investigate gastro-intestinal complaints during 18 days of Fermotein™ consumption. The secondary objective is to assess blood based parameters related to general health and consumer acceptance. The study has a randomized parallel design. Two different treatments will be evaluated e.g. a 18-day intervention with Fermotein™ based meals and a 18-day intervention with control meals. At the start and at the end of the intervention a blood sample will be collected. Questionnaires about gut complaints, stool consistency and frequency, wellbeing, health complaints or other adverse effects will be collected daily during intervention and up to two days after the intervention.

Interventions

OTHERFermotein based meals

various meal products: bread, soup and an occasional burgers

OTHERMatching control meals with whey protein and wheat bran

various meal products: bread, soup and an occasional burgers

Sponsors

The Protein Brewery
CollaboratorUNKNOWN
Wageningen University and Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Apparently healthy men and women (based on questionnaire) * Age between 18 and 70 years * Body mass index (BMI) between 18.5 and 29.9 kg/m2

Exclusion criteria

* Any metabolic, gastrointestinal, inflammatory or chronic disease (such as diabetes, anaemia, hepatitis, cardiovascular disease), judged by the medical doctor * History of gastro-intestinal surgery or having (serious) gastro-intestinal complaints * History of liver dysfunction (cirrhosis, hepatitis) * Kidney dysfunction (self reported) * Use of medication that may influence the study results, such as gastric acid inhibitors or laxatives * Reported slimming or medically prescribed diet * Current smokers * Alcohol intake over 4 glasses of alcoholic beverages per day * Pregnant, lactating or wishing to become pregnant in the period of the study (self-reported) * Abuse of illicit drugs * Having food allergies * Participation in another clinical trial at the same time * Being an employee of the department Consumer Science and Health group of Wageningen Food and Biobased Research

Design outcomes

Primary

MeasureTime frameDescription
Change in gastro intestinal (GI) complaintsDaily, during 18 days of Fermotein™ intake and up to three days after intake.Determined by combining multiple outcome measures ( bloated feeling, belching, abdominal pain, flatulence, nausea, diarrhoea, constipation) measured via questionnaires with Visual Analogue Scale (VAS) scores; from no complaints (minimal) to serious complaints (maximum). Higher values represent a worse outcome.

Secondary

MeasureTime frameDescription
change in blood Fe (iron)at baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood ferritinat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood insulinat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood glucoseat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood cholesterol (total)before and after 18 days consumption of Fermotein™ or control productunder fasting conditions
change in blood ALATat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood hemoglobinat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood GGTat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood leukocyte cell countsat baseline, and after 18 days of fermotein or control product consumptionunder fasting conditions
change in blood creatinineat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood zonulinat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions
change in blood pressureat baseline, and after 18 days of Fermotein™ or control product consumptionsystolic and diastolic bloodpressure
change in blood ASATat baseline, and after 18 days of Fermotein™ or control product consumptionunder fasting conditions

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026