Effect on Oral-cardio Health From Dietary Nitrate Loaded Functional Gum

Sponsor
University of Maryland, Baltimore (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06029283
Collaborator
(none)
30
2
9

Study Details

Study Description

Brief Summary

The purpose of this research is to determine the effects of a chewing gum containing dietary nitrate to your gingival and heart health. Dietary nitrates are commonly found in leafy vegetables and beets. The information learned from the study may help us further understand the interconnection of oral health and heart health. The study is looking for individuals who present with mild to moderate gum irritation or bleeding.

In the study participants will be randomized into either a group that will use a chewing gum containing dietary nitrate, or use a placebo chewing gum during a three-week period.

Participants in the study will have a simple gingival exam, x-rays if needed, and small samples of saliva and blood collected. All participants will also undergo a routine tooth cleaning. Participants will be asked to breathe in a tube to sample the levels of nitric oxide. Finally, participants will have their heart health measured with a device that is like a blood pressure cuff.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: dietary nitrate
  • Other: Placebo chewing gum
N/A

Detailed Description

The purpose of the project is to characterize, in subjects with gingival inflammation, the effect of a prebiotic dietary nitrate formulated chewing gum on the oral microbiome. In order to assess this, we will observe gingival health and parameters related to vascular health:

We are testing the hypothesize that short term use of functional gum will have improved inflammatory measures of the gingiva and beneficial cardiovascular impact. We endeavor to discover if any observed changes to oral and cardiovascular measures may be associated to changes to oral microbiome composition.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
Effect on Oral-cardio Health From Dietary Nitrate Loaded Functional Gum
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo arm of non-dietary nitrate gum

Placebo gum with no dietary nitrate

Other: Placebo chewing gum
placebo chewing gum

Experimental: Test arm of dietary nitrate containing gum

Functional gum with dietary nitrate

Dietary Supplement: dietary nitrate
dietary nitrate in a chewing gum delivery vehicle

Outcome Measures

Primary Outcome Measures

  1. Gingival inflammation [0 and 21 days]

    Gingival index or similar data collected.

  2. Microbiome profile [0 and 21 days]

    salivary sample collected

  3. Blood vessel elasticity [0 and 21 days]

    CV profiler device used

  4. nitric oxide [0 and 21 days]

    Breathalyzer type test

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Adult subjects with mild to moderate gingivitis, as defined with a MGI score of at least 2.0 Subjects must have a minimum of 20 natural teeth Subjects must able to chew gum

Exclusion Criteria:

Significant alveolar bone loss (>3.0 mm CEJ to bone) Requirement for antibiotic pre-medication prior to dental procedures Systemic antibiotic use in past 14 days to current. Use of anti-inflammatory (NSAIDs) or in past 14 days Use of anticoagulant therapy or in past 14 days. Current smokers Pregnancy Use of any oral rinses such as, but not limited to chlorhexidine, essential oils, cetylpyridinium chloride during the study.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Maryland, Baltimore

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Maryland, Baltimore
ClinicalTrials.gov Identifier:
NCT06029283
Other Study ID Numbers:
  • HP-00106795
First Posted:
Sep 8, 2023
Last Update Posted:
Sep 8, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 8, 2023