CClinicalTrials.gg
RecruitingNCT07572513Updated May 7, 2026

Slowly Digestible Carbohydrates for GLP-1 Secretion

An interventional study of Maltodextrin (Placebo) and Raw Corn Starch in Blood Glucose, GLP-1 and Satiety, sponsored by Purdue University. Recruiting at 1 site in United States. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-07.

Sponsored by Purdue University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
19
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
All
01

Study summary

The goal of this clinical trail is to learn if the hormone, glucagon-like peptide-1 (GLP-1), is stimulated by slowly digestible carbohydrates (SDCs) in healthy adults. In the current study, researchers will observe the amount of SDC that results in clinically meaningful levels of GLP-1, shown by an increase in feelings of fullness and a decrease in hunger, and how long an elevated level of GLP-1 lasts after starch consumption. Researchers aim to address two questions: What amount of SDC maximizes GLP-1-mediated satiety, and does the impact to satiety continue in a second meal? The overall goal is to maximize ileal-digesting SDC's potential use as a food-based agent for weight loss.

Researchers will compare 20, 40, and 60 g of raw corn starch compared to a maltodextrin control on total plasma GLP-1 concentrations, insulin, and blood glucose at baseline and 15, 30, 60, 90, 120, and 180 minutes post-consumption of SDC. Researchers will also measure satiety at baseline, 60, 120, 180 minutes and after a second meal.

There will be a total of 4 study visits with a least a 7-day break between visits. At each study visit, participants will:

  • Consume a randomized test beverage (SDC or maltodextrin)
  • Receive a blood draw at 7 timepoints over 3 hrs
  • Take a satiety questionnaire 5 times over 3 hrs
  • Consume a standardized lunch 3 hrs after the test beverage consumption
02

Conditions studied

  • Blood Glucose
  • GLP-1
  • Satiety
  • Second Meal Intake
  • Healthy Participant Study

Keywords

  • GLP-1
  • Slowly-Digestible Starch
  • Ileal-Digesting Starch
  • Dietary Starch
  • Satiety
  • Starch
  • raw corn starch
  • Blood Glucose
03

In context

Lead sponsor

Purdue University is the lead sponsor of 168 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Healthy population
  2. BMI between 18.5 and 24.9 kg/m2
  3. Adults 18 - 45 years old
  4. Men or women
  5. Able to read/speak English
  6. Fasting blood glucose levels ≤100 mg/dL
  7. HbA1c ≤ 5.7%

Exclusion criteria

Exclusion Criteria:

  1. Participants with 18 > Years of Age > 45 will be excluded.
  2. Subjects with 18.5 kg/m² > BMI > 24.9 kg/m² will be excluded.
  3. Diabetic individuals will be excluded.
  4. Individuals with history of gastrointestinal disease will be excluded from the study.
  5. Pregnant or nursing women will also be excluded.
  6. Individuals taking GLP-1 medications, or on weight-loss diets or restrictive eating patterns.
  7. Individuals suffering from dairy or gluten intolerance or allergies will be excluded.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
19 participants (estimated)

Study arms

  • Placebo comparator
    Maltodextrin

    Maltodextrin increases GLP-1 from 0-60 minutes but doesn't have an extended or elevated plasma GLP-1 into 2-3 hrs post-consumption. Participants will consume a treatment that is either entirely maltodextrin or partially maltodextrin during each of the 4 study visits.

    Dietary Supplement: Maltodextrin (Placebo)

  • Experimental
    Low-Dose SDC

    20 g of raw corn starch (SDC) + 55g of maltodextrin = 75 g total Researchers hypothesize that raw corn starch will have an extended or elevated plasma GLP-1 into 2-3 hrs post-consumption. Participants will consume the low-dose once during one of the study visits.

    Dietary Supplement: Maltodextrin (Placebo) · Dietary Supplement: Raw Corn Starch

  • Experimental
    Medium-Dose SDC

    40 g of raw corn starch (SDC) + 35g of maltodextrin = 75 g total Researchers hypothesize that raw corn starch will have an extended or elevated plasma GLP-1 into 2-3 hrs post-consumption. Participants will consume the medium-dose once during one of the study visits.

    Dietary Supplement: Maltodextrin (Placebo) · Dietary Supplement: Raw Corn Starch

  • Experimental
    High-Dose SDC

    60 g of raw corn starch (SDC) + 15g of maltodextrin = 75 g total Researchers hypothesize that raw corn starch will have an extended or elevated plasma GLP-1 into 2-3 hrs post-consumption. Participants will consume the high-dose once during one of the study visits.

    Dietary Supplement: Maltodextrin (Placebo) · Dietary Supplement: Raw Corn Starch

Interventions

  • Dietary supplementMaltodextrin (Placebo)

    75 g of maltodextrin diluted in 200 mL of water, taken once at a study visit

    Also known as: Control

  • Dietary supplementRaw Corn Starch

    Quantity of raw corn starch will vary between low, medium, and high-dose treatment arms (20, 40, 60 g respectively). Each treatment will total 75 g using maltodextrin to account for mass difference (55, 35, 15 g respectively).

    Also known as: Slowly-Digestible Carbohydrate, Ileal-Digesting Starch

06

What researchers measure

Primary outcomes

  1. Total GLP-1 Secretion

    To determine the impact of 20, 40, 60 g of SDC compared to a maltodextrin control on total plasma GLP-1 concentrations at baseline and 15, 30, 60, 90, 120, and 180 minutes post-consumption of SDC. Assessed via spun blood plasma and ELISA Total GLP-1 Kits.

    Time frame: From baseline and 15, 30, 60, 90, 120, and 180 minutes post-consumption of treatment for each participant over the course of the 4 arms.

Secondary outcomes

  1. Satiety

    Measure satiety at baseline, 60, 120, 180 minutes and after a second meal via satiety questionnaires

    Time frame: From baseline, 60, 120, 180 minutes and after a second meal for each participant over the course of the 4 arms.

  2. Blood Glucose

    To determine the impact of 20, 40, 60 g of SDC compared to a maltodextrin control on total plasma glucose concentrations at baseline and 15, 30, 60, 90, 120, and 180 minutes post-consumption of SDC. Assessed via spun blood serum.

    Time frame: From baseline, and 15, 30, 60, 90, 120, and 180 minutes post-consumption for each participant over the course of the 4 arms

  3. Insulin

    To determine the impact of 20, 40, 60 g of SDC compared to a maltodextrin control on insulin concentrations at baseline and 15, 30, 60, 90, 120, and 180 minutes post-consumption of SDC. Assessed via spun blood plasma.

    Time frame: From baseline, and 15, 30, 60, 90, 120, and 180 minutes post-consumption for each participant over the course of the 4 arms

07

Study locations

1 of 1 sites recruiting
  • Clinical Research Center at Purdue University
    West Lafayette, Indiana 47907, United States
    Recruiting
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Apr 14, 2026
  • Informed consent form · Apr 14, 2026
  • Informed consent form · Apr 14, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07572513
Lead sponsor
Purdue University
Responsible party
Bruce R. Hamaker (Principle Investigator, Purdue University) — Principal investigator
First posted
May 7, 2026
Start date
May 1, 2026 (estimated)
Primary completion
Jul 30, 2026 (estimated)
Completion
Nov 25, 2026 (estimated)
Last update
May 7, 2026

Study contacts

Bruce R Hamaker, Ph.D.
Contact
hamakerb@purdue.edu
765-494-5668
Erica de Jong, B.s.
Contact
dejonge@purdue.edu
7654963802

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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