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RECRUITINGOBSERVATIONAL

Associations Between the Microbiome, Skeletal Muscle Perfusion, and Fitness Status

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The purpose of the study is to determine associations between fitness status, bacteria in the mouth, and the blood flow to muscle. This study is trying to find out if fitness status impacts the bacteria that are present in the oral microbiome (environment in the mouth) or the ability of the body to send blood to the skeletal muscle. Participants will complete all or some of the following: * A mouth swab to assess the bacteria in their mouths. * Produce a saliva sample into a tube. * Cycle on a bike until you reach maximum effort. * Undergo blood draws * Wear a 24-hour non-invasive device that monitors blood pressure. * Drink 70mL (1/3 of a cup) of concentrated beetroot juice once

Who May Be Eligible (Plain English)

Who May Qualify: - Subjects must be able to communicate meaningfully with the investigator and must be legally competent to provide written willing to sign a consent form. - Subjects may be of either sex with age 18 years. Who Should NOT Join This Trial: - Oral antibiotic use within previous four weeks - Oral disease or poor oral health as determined by the Oral Health Questionnaire - Using an antibacterial mouthwash or a mouthwash containing chlorhexidine and unwilling to discontinue use - Tobacco smokers - Pregnant or lactating females - Hypersensitivity to any ultrasound contrast agent - Inability to perform exercise - Unable to communicate effectively in English to the study team. - Diagnosis of chronic renal failure (GFR \< 60 ml/min/1.73m) - Subjects taking nitroglycerine (or inorganic nitrates), PDE-5 inhibitors (ex: Cialis, Viagra), and xanthine oxidase inhibitors (ex: Allopurinol). Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Subjects must be able to communicate meaningfully with the investigator and must be legally competent to provide written informed consent. * Subjects may be of either sex with age 18 years. Exclusion Criteria: * Oral antibiotic use within previous four weeks * Oral disease or poor oral health as determined by the Oral Health Questionnaire * Using an antibacterial mouthwash or a mouthwash containing chlorhexidine and unwilling to discontinue use * Tobacco smokers * Pregnant or lactating females * Hypersensitivity to any ultrasound contrast agent * Inability to perform exercise * Unable to communicate effectively in English to the study team. * Diagnosis of chronic renal failure (GFR \< 60 ml/min/1.73m) * Subjects taking nitroglycerine (or inorganic nitrates), PDE-5 inhibitors (ex: Cialis, Viagra), and xanthine oxidase inhibitors (ex: Allopurinol).

Locations (1)

UVA Student Health and Wellness Building
Charlottesville, Virginia, United States