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Completed

NCT Number: NCT04095442

Effect of Antibacterial Mouthwash on Muscle Function in Healthy Young Men and Women

The purpose of this study is to determine the effects of antibacterial mouthwash on muscle speed and power in healthy young men and women. We have previously demonstrated that drinking beetroot juice, a source of dietary nitrate and therefore nitric oxide, increases muscle function in this population. Antibacterial mouthwash has been shown to interfere with the conversion of dietary nitrate to nitric oxide. We therefore hypothesize that it will diminish nitric oxide bioavailability and inhibit muscle contractility.

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Key information

Conditions

Age range

18 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Indiana University School of Health and Human Sciences

Indianapolis, Indiana, 46202, United States

About this study

Study Visit One:

During an initial visit, subjects will complete the informed consent process, be instructed on the requirements of the study, and practice the exercise protocol (see below).

Study Visit Two:

Subjects will be tested after they have avoided exercise, caffeine, alcohol, chewing gum, and foods high in nitrate (e.g., spinach, beets, collard greens) for at least 24 hours. They will also be asked to not use any mouthwash products during this period. They will then provide provide a saliva sample for subsequent measurement of nitrate and nitrite concentrations and have their breath nitric oxide levels measured using a portable analyzer. The maximal knee extensor speed and power of their knee extensor muscles will then be measured using an isokinetic dynamometer. This machine can control the speed of movement while measuring the maximal force (torque) that a subject can voluntarily produce.

Subjects will then be randomly assigned to receive either an antibacterial mouthwash (Cepacol©, Reckitt Benckiser, Parsippany, NJ) or, as a control solution, an alcohol-free "natural" mouthwash (Tom's of Maine©, Kennebunk, ME). Participants will be asked to rinse their mouth as directed on the product's packaging for 30 s twice per day for 7 (+/-2) days and to record the usage of the mouthwash on a provided form. Subjects will then return for Study Visit 3 (see below). This is considered a single-blind study, which means that the investigators will not know what type of mouthwash a subject is receives.

Study Visit Three:

At the end of the treatment period, subjects will be asked to return to undergo the same procedures as described for Study Visit Two.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion:

  • Men and Women age 18-30 years old
  • No current use of mouthwash

Exclusion:

  • Men and Women <18 or 30> y of age
  • Unable to provide informed consent
  • Current users of mouthwash
  • Current antibiotic use
  • Current smokers
  • Currently pregnant or lactating
  • Stage II hypertension (resting blood pressure >140/>90)

An answer of yes to any of the seven questions on the first page of the Physical Activity Readiness Questionnaire (PAR-Q) indicating that the subject is not physically ready for exercise without a medical exam. These exclusions include the following:

  • If participant's doctor has ever said that he/she has a heart condition and that he/she should only do physical activity recommended by a doctor
  • Pain in chest when doing physical activity
  • In past month, chest pain when not doing physical activity
  • If participant has ever lost balance because of dizziness or has ever lost consciousness
  • Bone or joint problem that could be made worse by change in physical activity
  • Currently on prescribed drugs for blood pressure or heart condition.
  • If the participant knows of any other reason why he/she should not do physical activity.

Treatment and study plan

Cepacol

Device

Twice-daily use of Cepacol per the manufacturer's guidelines

Tom's Natural Mouthwash

Device

Twice-daily use of Tom's Natural Mouthwash per the manufacturer's guidelines

Primary outcomes

  1. Muscle Function

    Time frame: 1 day

    Maximal knee extensor speed determined using isokinetic dynamometry

  2. Muscle Function

    Time frame: 7 day

    Maximal knee extensor speed determined using isokinetic dynamometry

Secondary outcomes

  1. Salivary Nitrate

    Time frame: 1 day

    Salivary concentration of nitrate

  2. Salivary Nitrite

    Time frame: 7 day

    Salivary concentration of nitrite

  3. Breath Nitric Oxide

    Time frame: 1 day

    Breath nitric oxide level

  4. Breath Nitric Oxide

    Time frame: 7 day

    Breath nitric oxide level

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Registry information

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Sep 19, 2019
Registry last updated
Mar 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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