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Clinical Trials/NCT03823222
NCT03823222CompletedNot Applicable

Proteins From Duckweed Trial

Wageningen University and Research2 sites in 1 country12 target enrollmentStarted: February 28, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
12
Locations
2
Primary Endpoint
Change in blood free amino acids (e.g. Degree of digestibility)

Study Overview

Brief Summary

This study aims to study the digestibility of isolated duckweed protein. The digestibility of the isolated duckweed protein will be compared to an isolated benchmark protein whey.

Objective: The primary objective is to investigate the digestibility of isolated duckweed protein and the isolated benchmark protein whey.

Study design: The study is a cross-over, double blind, controlled trial in which study participants will visit the research facility on two occasions under fasting conditions. Subjects will receive two protein sources in randomized order with a washout period of one week. Blood will be collected via a catheter before and up-to 3 hours after protein consumption.

Study population: We aim to include 12 healthy volunteers aged 18-50 years. Intervention: Study participants will receive 20 grams of isolated duckweed protein and the isolated benchmark protein whey.

Main study parameters/endpoints: The main study parameter is blood amino acids measured before and after consumption of 20 g protein.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Body mass index (BMI) between 18 and 25 kg/m2
  • Having veins suitable for blood sampling via a catheter (judged by study nurse/ medical doctor)

Exclusion Criteria

  • Any metabolic, gastrointestinal, inflammatory or chronic disease (such as diabetes, anaemia, hepatitis, cardiovascular disease)
  • History of gastro-intestinal surgery or having (serious) gastro-intestinal complaints
  • History of liver dysfunction (cirrhosis, hepatitis) or liver surgery
  • Kidney dysfunction (self-reported)
  • Use of medication that may influence the study results, such as gastric acid inhibitors, laxatives, stomach protectors and drugs that can affect intestinal motility
  • Anaemia (Hb values <7.5 for women and <8.5 for men)
  • Reported slimming, medically prescribed, vegan/vegetarian or other extreme diets or the use of protein supplements
  • Not willing to give up blood donation during the study
  • Current smokers
  • Alcohol intake ≥4 glasses of alcoholic beverages per day
  • Pregnant, lactating or wishing to become pregnant in the period of the study (self-reported)
  • Abuse of illicit drugs
  • Food allergies for products that we use in the study
  • Participation in another clinical trial at the same time
  • Being an employee of the department Consumer Science & Health group of Wageningen Food & Biobased Research

Arms & Interventions

Duckweed protein

Experimental

20 gram of isolated protein

Intervention: Duckweed protein (Dietary Supplement)

Whey protein

Experimental

20 gram of isolated protein

Intervention: Whey protein (Dietary Supplement)

Outcomes

Primary Outcomes

Change in blood free amino acids (e.g. Degree of digestibility)

Time Frame: 20 gram protein will be consumed and blood samples will be taken before and up to 3 hours after protein consumption

postprandial test, determine free amino acids in blood samples collected before and after a postprandial challenge test

Secondary Outcomes

  • change in plasma glucose(20 gram protein will be consumed and blood samples will be taken before and up to 3 hours after protein consumption)
  • change in plasma insulin(20 gram protein will be consumed and blood samples will be taken before and up to 3 hours after protein consumption)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Diederik Esser

project leader clinical trials

Wageningen University and Research

Study Sites (2)

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