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Determination of In-vivo Plasma AA Appearance From Plant Protein Fibre Products

NCT05420142 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2022-09-26

No results posted yet for this study

Summary

This study aims to assess the digestibility and efficacy of the study groups previously developed innovative plant-based protein and fibre products.

Conditions

  • Aging
  • Undernutrition
  • Appetite Loss
  • Age-Related Sarcopenia

Interventions

DIETARY_SUPPLEMENT

Net peripheral AA appearance following ingestion of 3 selected PPF products compared to whey

The intervention will assess the effects of three difference varieties of plant-based protein and fibre supplements on net peripheral amino acid appearance in blood compared to whey protein with matched fibre content as a control arm.

Sponsors & Collaborators

  • Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement

    collaborator OTHER

  • University of Padova

    collaborator OTHER

  • Fraunhofer Institute for Interfacial Engineering and Biotechnology

    collaborator OTHER

  • University College Dublin

    lead OTHER

Principal Investigators

  • Helen Roche, Prof · University College Dublin

  • Katy Horner, Dr · University College Dublin

  • Dominique Dardevet, Dr · Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE)

  • Giuseppe De Vito, Prof · University of Padua Department of Biomedical Science, Neuromuscular Physiology Laboratory

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-14
Primary Completion
2022-05-12
Completion
2022-07-31

Countries

  • Ireland
  • Italy

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 NCT05420142 on ClinicalTrials.gov