Periodontal Disease and Salivary Mitofusin Levels

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorErzincan University

About this trial

The aim of this observational study is to find out whether there is a level difference in salivary mitofusin-1 and mitofusin-2 levels due to changes in periodontal status. The main question it aims to answer is:

* Do salivary mitofusin-1 and mitofusin-2 levels of periodontitis patients differ from healthy patients? * Could salivary mitofusin-1 and mitofusin-2 levels be biomarkers for periodontal disease?

Biochemical analysis will be performed on saliva samples taken at once from gingivitis or periodontitis patients and healthy individuals who apply to the periodontology clinic, at the initial stage of the treatment. There is no ongoing monitoring or second sampling.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Being between the ages of 18 and 65.

Willing to participate in the study and provide a saliva sample.

Having a healthy periodontal condition, gingivitis, or periodontitis (Stage 3-4, Grade C).

Having fasted from any food or drink (except water) for the past 2 hours prior to providing the saliva sample.

Disqualifiers

Having used antibiotics within the last 6 months.

Having received periodontal treatment within the last 6 months.

Having fewer than 20 teeth (excluding third molars).

Having any systemic diseases.

Trial population

Patients with gingivitis and periodontitis presenting to the periodontology clinic, as well as healthy individuals

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • Biochemical analysis of saliva sample

    Diagnostic test

    It is the examination of saliva samples taken with biochemical methods. In this way, the substances in its content and the concentration of cytokines are analyzed.

Treatment groups

81 Participants
are divided into 3 treatment groups
Group A: Healthy1 intervention
Group B: Gingivitis1 intervention
Group C: Periodontitis1 intervention

Trial outcomes

Primary outcomes

1

Mitofusin-1 concentration

Mitofusin-1 concentration in saliva, determined as a result of biochemical analysis

Time frame
Up to four weeks from start of work
2

Mitofusin-2 concentration

Mitofusin-2 concentration in saliva, determined as a result of biochemical analysis

Time frame
Up to four weeks from start of work
3

IL-1B concentration

IL-1B concentration in saliva, determined as a result of biochemical analysis

Time frame
Up to four weeks from start of work

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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