Effects of Pea Proteins With Different Degrees of Processing on Postprandial Metabolism in Healthy Adults

NCT06155656 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-04-23

No results posted yet for this study

Summary

The aim of this study is to investigate the postprandial metabolic responses to plant-based protein ingredients of different degrees of processing (pea protein concentrate, isolate, and extrudate) and in comparison to whey protein in healthy adults. Therefore, young healthy subjects consume 4 test meals with 25 g of protein from pea protein concentrate, pea protein isolate, pea protein extrudate or whey protein in a randomized order. In a postprandial period of 6 hours, parameters of protein and glucose metabolism (i.a. plasma amino acids), gastric emptying and hunger/satiety are analysed. It is assumed that the plasma amino acid profile after plant protein ingestion differs depending on processing level of the protein ingredients and in comparison to whey protein.

Conditions

  • Plasma Amino Acid Appearance and Disappearance
  • Postprandial Metabolic Events

Interventions

OTHER

Pea protein concentrate

Ingestion of a soup containing 25 g of protein from pea protein concentrate

OTHER

Pea protein isolate

Ingestion of a soup containing 25 g of protein from pea protein isolate

OTHER

Pea protein extrudate

Ingestion of a soup containing 25 g of protein from pea protein extrudate

OTHER

Whey protein

Ingestion of a soup containing 25 g of protein from whey protein

Sponsors & Collaborators

  • German Federal Ministry of Education and Research

    collaborator OTHER_GOV
  • University of Bonn, Department of Nutrition and Food Sciences, Food Sciences

    collaborator UNKNOWN
  • University of Bonn

    lead OTHER

Principal Investigators

  • Sarah Egert, Prof PhD · Germany University of Bonn

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-22
Primary Completion
2024-06-28
Completion
2024-06-28

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06155656 on ClinicalTrials.gov