Status:

COMPLETED

Effect of Degree of Polymerization and Linkage of α-glucans on Post-prandial Glucose Response

Lead Sponsor:

Société des Produits Nestlé (SPN)

Conditions:

Postprandial Glucose Response

Eligibility:

All Genders

18-45 years

Phase:

NA

Brief Summary

The primary research project objective is to investigate whether a maltodextrin with high degree of polymerization (Roquette Glucidex 2) and a dextran with comparable degree of polymerization (Pharmac...

Detailed Description

The aim of the present research project is to generate comparative data on post-prandial glucose response (PPGR) of α-glucans varying systematically degree of polymerization and linkage type. These da...

Eligibility Criteria

Inclusion

  • Male and female participant
  • Healthy status (based on anamnesis)
  • Age between 18 and 45 years
  • BMI between 18.5 and 29.9 kg/m2
  • Able to understand and sign an informed consent form
  • Able to respect the study procedures and timelines
  • Swiss resident living in canton Fribourg (French part), Neuchâtel, Vaud and Valais which is in the competence of Ethical Committee of Vaud
  • Having wireless internet access at home

Exclusion

  • Any known metabolic disease including diabetes or drug chronic intake (aspirin, vitamin C and mineral supplements, steroids, protease inhibitors, antidepressants, anxiolytic, or antipsychotics…) possibly impacting (to the opinion of the medical responsible): The digestion or absorption of nutrients, the postprandial glucose response
  • Major medical/surgical event requiring hospitalization in the last 3 months
  • Pregnancy or lactation
  • Known food allergy and intolerance
  • Medically known cutaneous hypersensitivity to adhesives, silicon watch-strap and plasters
  • Alcohol intake higher than 2 servings per day. A serving is 0.4 dl of strong alcohols, 1 dl of red or white wine, or 3 dl of beer.
  • Smokers
  • Participant having a hierarchical link with the research team members

Key Trial Info

Start Date :

November 29 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 18 2020

Estimated Enrollment :

10 Patients enrolled

Trial Details

Trial ID

NCT05266690

Start Date

November 29 2019

End Date

February 18 2020

Last Update

March 4 2022

Active Locations (1)

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Nestlé Research - Clinical Research Unit - Clinical Innovation Lab

Lausanne, Canton of Vaud, Switzerland, 1000