Actively Recruiting

Age: 10Years - 18Years
All Genders
Healthy Volunteers
NCT07236125

Dietary Nitrate and the Oral Microbiome in Children With Primary Hypertension

Led by Yelda Kasımoğlu · Updated on 2026-05-08

48

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

Sponsors

Y

Yelda Kasımoğlu

Lead Sponsor

I

Istanbul University Scientific Research Projects Coordination Unit- Pending

Collaborating Sponsor

AI-Summary

What this Trial Is About

Children and adolescents with primary hypertension (high blood pressure without an underlying secondary cause) are at increased risk of cardiovascular disease in adulthood. Recent research suggests that not only the heart and blood vessels, but also the bacteria living in the mouth may play a role in blood pressure regulation. Certain oral bacteria can convert nitrate from food into nitrite and then into nitric oxide, a substance that helps blood vessels relax. If this nitrate-nitrite-nitric oxide pathway is impaired, blood pressure may rise. This study aims to investigate the relationship between oral microbiota, salivary nitric oxide reductase activity and blood pressure in children and adolescents with primary hypertension compared with healthy peers. We will recruit participants aged 10-18 years who have a diagnosis of primary hypertension and an age- and sex-matched control group without hypertension. All participants will undergo a non-invasive oral and dental examination and standardized blood pressure measurements. Saliva samples will be collected to measure pH, flow rate, nitrate and nitrite levels, total protein, lysozyme activity and to analyze the composition of oral bacteria using modern DNA-based techniques. Participants and/or their parents will also complete brief questionnaires about diet and general health. No medication or dietary supplement will be given as part of the study, and no additional blood samples will be taken beyond routine clinical care. The main risk is minimal discomfort related to oral examination and saliva collection. There is no guaranteed direct benefit for participants; however, the results may help us better understand how oral bacteria and salivary nitric oxide pathways are linked to high blood pressure in young people. This knowledge may support the development of new non-invasive strategies for early detection and prevention of hypertension in the future.

CONDITIONS

Official Title

Dietary Nitrate and the Oral Microbiome in Children With Primary Hypertension

Who Can Participate

Age: 10Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Applied to the Istanbul University Faculty of Medicine, Department of Pediatric Nephrology
  • Between the ages of 10 and 18
  • Diagnosed with primary hypertension
  • Clinically excluded from secondary hypertension or heart failure
  • No systemic or chronic disease other than hypertension
  • No periodontal disease, dental infection, or oral mucosal disease
  • Not taking regular antihypertensive or other medications for a chronic disease
  • Not having received antibiotic treatment in the last 3 months
  • Patients who have not used mouthwash in the last 3 months
  • Have no allergies to nitrate-rich foods
  • Both male and female patients will be included.
Not Eligible

You will not qualify if you...

  • Younger than 10 years of age or older than 18 years of age
  • Clinically diagnosed with secondary hypertension or heart failure
  • Have a systemic disease
  • Have periodontal disease, dental infection, or oral mucosal disease
  • Are taking regular antihypertensive medications or other chronic illnesses
  • Have received antibiotic treatment within the last 3 months
  • Have used mouthwash within the last 3 months
  • Are allergic to nitrate-rich foods will not be included in the study.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Istanbul University Faculty of Dentistry

Istanbul, Fatih, Turkey (Türkiye), 34093

Actively Recruiting

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Research Team

Y

Yelda Kasimoglu Assoc. Prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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