Skip to content

Gum Acacia and Blood Glucose

The Effect of Gum Acacia on Satiety, Glycemic Response and Gastrointestinal Tolerance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03716479
Enrollment
48
Registered
2018-10-23
Start date
2018-10-09
Completion date
2019-09-01
Last updated
2019-10-04

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

Conditions

Diet Modification

Brief summary

This study will provide needed insight on the satiety and blood glucose and l effects of the soluble fiber gum acacia at 20g and 40g doses.

Detailed description

This is a randomized, single-blind, crossover, intervention study testing the satiety and blood glucose effects of the soluble fiber gum acacia.

Interventions

20 g of acacia gum will be added to orange juice

40 g of acacia gum will be added to orange juice

No acacia gum will be added to orange juice.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Masking description

fiber will be mixed into orange juice

Intervention model description

subjects will consume 0, and 2 doses of acacia gum

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

BMI between 18 and 29 kg/m2

Exclusion criteria

* distaste for bagels and cream cheese, orange juice or cheese pizza; * current smoker; * restrained eating habits; * recent weight change; * any history of disease or significant past medical history; * are vegetarian; * do not normally eat breakfast or lunch; * pregnant or lactating; * irregular menstrual cycles.

Design outcomes

Primary

MeasureTime frameDescription
Blood glucose levels0, 30, 60, 120, 180, and 240 minutes after breakfast; Area under the curve (AUC) will be calculated for each treatmentBlood will be taken via finger stick
Appetite Sensation15, 30, 45, 60, 90, 120, 180 and 240 minutes after breakfast; Area under the curve (AUC) will be calculated for each treatmentSubjective visual analog scale (VAS) will be utilized to assess hunger, fullness and desire to eat

Countries

United States

Outcome results

None listed

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