ClinicalTrials.Veeva

Menu

Satiety Response of Four Dietary Fibers

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status and phase

Completed
Early Phase 1

Conditions

Healthy

Treatments

Dietary Supplement: Soluble corn fiber
Dietary Supplement: Control
Dietary Supplement: Fructooligosaccharide
Dietary Supplement: Resistant starch
Dietary Supplement: Inulin

Study type

Interventional

Funder types

Other

Identifiers

NCT01233024
1003E78714

Details and patient eligibility

About

Studies have found a relationship between dietary fiber consumption and body weight regulation. This relationship may stem from enhanced satiety through fermentation of certain fibers in the large intestine.

The objective of this study is to determine and compare satiety ratings, changes in food intake, and gastrointestinal effects for four fibers: fructooligosaccharide, inulin, soluble corn fiber, and resistant starch.

Enrollment

20 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy women
  • Age 18-40 years
  • Nonsmoking
  • Not taking weight loss medications
  • Non-dieting (weight has not changed more than 11 pounds over three months)
  • BMI between 18.5 and 29
  • Spoken and written English literacy

Exclusion criteria

  • Do not regularly consume breakfast
  • Food allergies to wheat, soy, peanut, or dairy
  • BMI less than 25 or greater than 29 upon admission to study
  • Cancer diagnosis in past 5 years
  • History of heart disease, kidney disease, diabetes, or eating disorder
  • History of ulcerative colitis, Crohn's disease, or any other gastrointestinal condition
  • History of drug or alcohol abuse in past 6 months
  • Use of lipid-lowering, anti-hypertensive, or anti-inflammatory steroid medication
  • Concurrent or recent (within 30 days) intervention study participation
  • Pregnant or lactating
  • Irregular menstrual cycle
  • Vegetarians
  • People who eat more than approximately 15 grams of fiber per day

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

20 participants in 5 patient groups, including a placebo group

Low fiber control
Placebo Comparator group
Description:
no treatment dinner bar, no treatment breakfast bar
Treatment:
Dietary Supplement: Control
Promitor soluble corn fiber
Experimental group
Description:
12g in dinner bar, 11g in breakfast bar
Treatment:
Dietary Supplement: Soluble corn fiber
FiberSym resistant starch
Experimental group
Description:
12g in dinner bar, 11g breakfast bar
Treatment:
Dietary Supplement: Resistant starch
Orafti P95 fructooligosaccharide
Experimental group
Description:
12g in dinner bar, 11g in breakfast bar
Treatment:
Dietary Supplement: Fructooligosaccharide
Orafti HPX inulin
Experimental group
Description:
12g in dinner bar, 11g in breakfast bar
Treatment:
Dietary Supplement: Inulin

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems