Pilot Study to Examine the Acute Impact of Veillonella Supplementation on Exercise and Lactate Re… (NCT05816291) | Clinical Trial Compass
CompletedNot Applicable
Pilot Study to Examine the Acute Impact of Veillonella Supplementation on Exercise and Lactate Responses
United States7 participantsStarted 2022-03-30
Plain-language summary
The purpose of this study is to assess the health and performance outcomes associated with supplementation of Veillonella atypica.
Who can participate
Age range18 Years – 50 Years
SexALL
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Inclusion Criteria:
* Provide voluntary signed and dated informed consent.
* Be in good health as determined by medical history and routine blood chemistries.
* Age between 18 and 50
* Exercises \> 150 mins/week
* Body Mass Index of 18.5-29.9 and Body Fat of 30%
* Normotensive (seated, resting systolic blood pressure \< 140 mm Hg and diastolic blood pressure \< 90 mm Hg. If the first measurement is slightly elevated above these limits, the subject will be given a brief (5 minute) rest period, and two more measurements will be taken. The average of all three measurements will be used to determine eligibility.
* Normal seated, resting heart rate (\< 90 beats per minute). Willing to follow all study protocols.
Exclusion Criteria:
* Individuals currently diagnosed or being treated for any cardiac, respiratory, endocrine, psychiatric, musculoskeletal, renal, hepatic, neuromuscular or metabolic disease or disorder that in the judgement of the study participant's personal physician or research nurse that will preclude their safe participation or will contraindicate quality control over the collected data
* Individuals currently diagnosed with or are being treated for celiac disease, lactose intolerance, digestive insufficiencies or other gastrointestinal complications such as irritable bowel syndrome, ulcerative colitis, etc.
* Alcohol consumption (more than 2 standard alcoholic drinks per day or more than 10 drinks per week) or drug abuse or dependence.
* Smokers or individuals …