Changes in Amino Acid Absorption After Adding a Probiotic to an Acute Protein Feeding
Completed · Not applicable
Conditions studied: Amino Acid Absorption
In brief
The purpose of this study is to examine the pharmacokinetic pattern of amino acid absorption after a two-week pattern of milk protein supplementation with and without the addition of Bacillus coagulans GBI-30, 6086.
Key facts
- Study ID
- NCT04427020
- Run by
- Lindenwood University
- People needed
- 30
- Starts
- 2019-08-08
- Expected to finish
- 2019-12-03
- Last updated by the study team
- 2020-06-11
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- All participants will be between the ages of 18-55 years.
- Participants will be healthy and free of disease as determined by evaluation of a medical history.
- Completing at least 30 minutes of moderate exercise three days per week
You may not qualify if…
- Those individuals less than 18 and greater than 55 years of age will be excluded.
- Any individual who is currently being treated for or diagnosed with a cardiac disorder or disease
- Any individual who is currently being treated for or diagnosed with a respiratory disorder or disease
- Any individual who is currently being treated for or diagnosed with a circulatory disorder or disease
- Any individual who is currently being treated for or diagnosed with a musculoskeletal disorder or disease
- Any individual who is currently being treated for or diagnosed with a metabolic disorder or disease
- Any individual who is currently being treated for or diagnosed with obesity (defined as body mass index > 30 kg/m and body fat greater than 30%)
- Any individual who is currently being treated for or diagnosed with an immune or autoimmune disorder or disease
- Any individual who is currently being treated for or diagnosed with a psychiatric disorder or disease
- Any individual who is currently being treated for or diagnosed with a hematological disorder or disease
- Any individual who is currently being treated for or diagnosed with a neurological disorder or disease
- Any individual who is currently being treated for or diagnosed with an endocrinological disorder or disease
- Participants who are determined to not be weight stable defined as measured body mass deviating by 2% or more.
- Participants who do not or are not willing to abstain from alcohol, nicotine, and caffeine for 12 hours prior to each visit will be excluded
- Participants who do not or are not willing to abstain from exercise for 12 hours prior to each visit will be excluded.
Where it is running
- Lindenwood University — Saint Charles, Missouri, United States
Full record on ClinicalTrials.gov
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