Clinical Trials Directory

Trials / Completed

CompletedNCT05963594

To Evaluate the Post-Prandial Metabolic Effects of Oligomalt in Adults With T2D and in HAO

A Randomized, Double-Blind, Comparator-Controlled, Crossover Study to Evaluate the Post-Prandial Metabolic Effects of Oligomalt in Adults With Type 2 Diabetes (T2D) and in Otherwise Healthy Adults With Overweight or Obesity (HAO)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
44 (actual)
Sponsor
Société des Produits Nestlé (SPN) · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The goal of this mechanistic, exploratory study is to compare the effectiveness of Oligomalt to Glucidex 40 after eating in adults with Type 2 Diabetes (T2D) and in otherwise healthy adults with overweight or obesity (HAO).

Detailed description

The main question it aims to answer is how consumption of Oligomalt, a slowly digestible carbohydrate, will reduce glucose and insulin spikes in adults with T2D and in HAO relative to Glucidex 40.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOligomaltThe investigational product (Oligomalt) dissolved in 300 ml water will be consumed over approximately 10 minutes in the morning of the study visit after a fasting period of at least 10 hours.
DIETARY_SUPPLEMENTmaltodextrinThe investigational product (maltodextrin) dissolved in 300 ml water will be consumed over approximately 10 minutes in the morning of the study visit after a fasting period of at least 10 hours.

Timeline

Start date
2023-01-23
Primary completion
2023-03-28
Completion
2023-03-28
First posted
2023-07-27
Last updated
2023-07-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05963594. Inclusion in this directory is not an endorsement.