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Nitrate Mouth Rinse and the Oral Microbiome

D

Dalhousie University

Status

Completed

Conditions

Oral Microbiome
Nitric Oxide

Treatments

Other: Water
Dietary Supplement: Beet Root

Study type

Interventional

Funder types

Other

Identifiers

NCT06588049
2024-7166

Details and patient eligibility

About

The study is aimed to determine if changes to the oral microbiome occur after the use of a nitrate rich mouth rinse. Participants with be asked to use either a controlled (water) mouthrinse once daily for 2 weeks while maintaining normal oral hygiene practices, or use the nitrate rich mouthrinse once daily for 2 weeks.

Primary Outcome measures:

-changes in the composition of the oral microbiome

Secondary Outcome measures

  • Blood Pressure
  • Salivary Nitric Oxide Levels

Full description

Nitrate is found in high concentrations in beet root, and as such we will use a beet root based product as a daily mouth rinse (Swish and Spit) as a part of the participants daily oral hygiene regimen and collect the participants biofilm before and after 2 weeks of regular use. We will then analyze the data using 16s rRNA sequencing to evaluate the changes in alpha diversity, beta diversity and the absolute and relative differential abundance of nitrate reducing bacteria in the oral microbiome. We will also collect salivary samples to evaluate NO levels, as well as measure blood pressure pre and post treatment.

After this study's completion, we expect to have gained new knowledge on nitrate's influence on the oral microbiome's composition. Gaining this knowledge will allow better public understanding of the effects oral hygiene products have on their oral and systemic health. In addition, the knowledge gained could encourage further investigations into how to better formulate oral hygiene products for improved health and performance.

Enrollment

21 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • You are between the ages of 18 and 40. Have no uncontrolled systemic diseases.

Participants with mild chronic conditions such as:

  • Asthma
  • Type 1 Diabetes Mellitus

Exclusion criteria

  • You are under the age of 18.

  • You have uncontrolled systemic diseases, or acute infections.

  • You are taking prescription, antibiotics, probiotics, or antimicrobial mouthrinses.

  • You have a documented true allergy (i.e Hives, Swelling of lips/throat) Soy, Nuts, Seeds, Dairy, Egg products, Fish/Shellfish or Wheat.

  • The presence of acute or chronic oral conditions including:

    • Herpes Simplex Virus (recent cold sores)
    • Stomatitis
    • Oral Lichen Planus
    • Angular Cheilitis
    • Candidiasis
    • Necrotizing Gingival Diseases
    • Other inflammatory or infectious pathologies
    • Active dental caries "cavities"
    • Any other periodontal diagnosis other than 'Healthy Periodontium' or localized gingivitis

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

21 participants in 2 patient groups, including a placebo group

Nitrate Mouth Rinse
Experimental group
Description:
Nitrate suspension with approximately 50-100mg nitrates formulated with water swished in mouth for 30 seconds and then expectorated once daily for 14 consecutive days.
Treatment:
Dietary Supplement: Beet Root
Water Mouth Rinse
Placebo Comparator group
Description:
Water mouth rinse swished in mouth for 30 seconds and then expectorated once daily for 14 consecutive days.
Treatment:
Other: Water

Trial contacts and locations

1

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Central trial contact

Leigha Rock; Jacob P Smith, DDS

Data sourced from clinicaltrials.gov

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