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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06045611
Other study ID # Dnr 2023-03852-01
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 13, 2023
Est. completion date May 2024

Study information

Verified date November 2023
Source Örebro University, Sweden
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this interventional study is to learn about the effects of different proteins (from animals or plants) on the metabolism in healthy, normal weight women between 18-45 year who are not on hormonal birth-control. The main questions the study aims to answer are: 1. How do different proteins affect biological markers of the metabolism and which protein has the strongest effect? 2. How are the different proteins digested and taken up from our body? Participants will drink four different shakes on four different study days in a random order. Three of them contain each a different protein and one does not contain protein. Right before drinking the shake and on 11 timepoints after drinking the shake blood samples will be drawn.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 28
Est. completion date May 2024
Est. primary completion date May 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Females - Age: 18-45 years - Body mass index: 18.5 < 25 kg/m2 - Signed informed consent Exclusion Criteria: - Use of hormonal contraceptives - Pregnancy or breastfeeding - Diabetes mellitus or any other metabolic disease that might affect the results of this study - Gastric surgery that affects digestion and uptake of protein - Any clinically significant present or past disease/condition and medication which in the investigator's opinion could interfere with the results of the trial

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Isolated Pea Protein
Participants will consume the protein supplement dissolved in water in an opaque mug wearing a nose clip.
Isolated Whey Protein
Participants will consume the protein supplement dissolved in water in an opaque mug wearing a nose clip.
Isolated Faba Bean Protein
Participants will consume the protein supplement dissolved in water in an opaque mug wearing a nose clip.
Placebo
Participants will consume the placebo in an opaque mug wearing a nose clip.

Locations

Country Name City State
Sweden Örebro University Örebro

Sponsors (1)

Lead Sponsor Collaborator
Örebro University, Sweden

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Release of Growth Hormone The primary outcome is defined as the postprandial release of growth hormone during three hours after oral ingestion of plant-protein test drinks vs. an animal-protein test drink measured as incremental area under the curve. Growth hormone will be measured in blood samples. 0-3 hours after consumption of test drink (on all 4 study days)
Secondary Release of Hormones Related to the Somatotrophic Axis We will measure different hormones related to the somatotrophin axis in collected blood samples and investigate if there are differences between different protein-sources. 0-3 hours after consumption of test drink (on all 4 study days)
Secondary Kinetics of Amino Acid Uptake We will measure amino acids in collected blood samples to investigate dynamics and kinetics of protein digestion/uptake of different protein sources. 0-3 hours after consumption of test drink (on all 4 study days)
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