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Fiber Tolerance Study

The Investigation of Gastrointestinal Tolerance of a Novel Fibre Blend Among ≥45-<70-year-old Men and Women

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06115057
Acronym
Gitomix
Enrollment
43
Registered
2023-11-02
Start date
2023-10-04
Completion date
2023-12-22
Last updated
2024-02-06

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

Conditions

Gastrointestinal Tolerance of Dietary Fiber

Keywords

Fiber Tolerance Gastro-intestinal Safety

Brief summary

Research shows that many people do not get enough dietary fiber through their normal diet. As a result, some nutrients are not properly absorbed into the bloodstream. The immune system however does need these nutrients. Dietary fibers are therefore important for health. Nutricia has developed a new blend of natural fibers that can help people get enough fiber.

Interventions

DIETARY_SUPPLEMENTFiber

Subjects in this study are to consume the study product twice daily during regular meals. The fiber mix consists of different types of dietary fiber that are individually well tolerated for human consumption.

Sponsors

NCRU (Nutrition Clinical Research Unit)
CollaboratorUNKNOWN
Nutricia Research
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

open-label, single-arm, single-site

Eligibility

Sex/Gender
ALL
Age
45 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age ≥ 45 and ≤ 70 years 2. Body Mass Index (BMI) ≥ 18.5 and ≤ 29.9 kg/m2 3. Signed consent form 4. Willingness and ability to comply with the protocol 5. Good general health 6. Defecation frequency: between three bowel movements per week and three bowel movements per day within a month for screening.

Exclusion criteria

1. Presence or history of chronic gastrointestinal disorders (e.g. stomach ulcers, ulcerative colitis, Crohn's disease) or history of abdominal surgery with resection of the bowel (small or large intestine). 2. Presence of other medical conditions where gastrointestinal function often/probably is affected, such as: 1. autoimmune diseases (e.g. diabetes mellitus type I, multiple sclerosis, systemic lupus erythematosus). 2. eating disorders (e.g. anorexia nervosa, bulimia nervosa, binge eating disorder). 3. intestinal/gastrointestinal disorder due to a stroke. 3. Chronic diseases (including but not limited to hypertension, dyslipidaemia, type 2 diabetes mellitus, thyroid disorders) that cannot be controlled with the use of medication/therapy. 4. Severe acute liver disease or chronic liver disease. 5. Severe or chronic kidney disease or need for hemodialysis. 6. Colonoscopy, irrigoscopy or other bowel cleansing, or other surgical procedures related to the gastrointestinal tract (eg. colon polypectomy, appendectomy) or for which use of systemic antibiotics within 1 month before the screening is required or scheduled during participation in the study. 7. Use of enemas, laxatives, antacids, proton pump inhibitors, prokinetics (e.g. metoclopramide, drugs that affect motility), digestive enzymes, narcotic/morphine analgesics within 1 week prior to screening or intended use during participation in the study. 8. Following a vegetarian or vegan diet.

Design outcomes

Primary

MeasureTime frameDescription
GSRS change4 weeksChange from baseline in the reported severity of GI symptoms assessed by the Gastrointestinal Symptom Rating Scale (GSRS) for diarrhea dimension at week 4 post-baseline.

Secondary

MeasureTime frameDescription
GSRS changeweek 1, week 2, week 3,Weekly changes from baseline in the reported severity of GI symptoms assessed by the GSRS for diarrhea dimension at week 1, week 2, and week 3 post-baseline.

Other

MeasureTime frameDescription
BSFCweek 1, week 4Weekly average faecal form type assessed by the Bristol Stool Form Chart at each defecation in the baseline week, at week 1, and week 4 post-baseline.
DQLQ4 weeksDigestion-associated Quality of life assessed by the Digestion-associated Quality of Life Questionnaire (DQLQ) at baseline and at week 4 post-baseline.
Stoolweek 2, week 3, week 4Microbiota and other outcome parameters assessed using collected faecal samples in the baseline week and every 7 days over 4 weeks post-baseline: * Composition, diversity, and abundance of microbiota using 16S rRNA gene sequencing and processing * Short-chain fatty acids (SCFA) * Branch-chain fatty acids (BCFA) * Lactate * Ammonia * Calprotectin * Secretory immunoglobulin A (sIgA) * pH
Defecation frequencyweek 1, week 2, week 3, week 4Weekly average frequency of defecation, derived from the number of faecal form types assessed by the Bristol Stool Form Chart.
GSRSweek 1, week 2, week 3, week 4The reported severity of GI symptoms assessed by the GSRS between week 1 v week 2, week 1 v week 3, week 1 v week 4, week 2 v week 3, week 2 v week 4, and week 3 v week 4 \[score\].

Countries

Netherlands

Outcome results

None listed

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