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Relationships Between Tenascin C, Smoking and Periodontal Status

N

Necmettin Erbakan University

Status

Not yet enrolling

Conditions

Periodontitis
Periodontal Diseases
Smoking

Treatments

Diagnostic Test: Clinical Measurements and Saliva Sample Collection

Study type

Observational

Funder types

Other

Identifiers

NCT06523205
tenascincsmokeperiodontitis

Details and patient eligibility

About

The goal of this observational study is to determine if there is a relationship between different periodontal conditions (gingival healthy, stage 2 grade B, stage 2 grade C, stage 3 grade B, stage 3 grade C) and the levels of tenascin C, IL-1 beta, IL-4, and IL-6 in saliva samples from smokers and non-smokers. The main questions it aims to answer are:

Is there a difference in the levels of tenascin C, IL-1 beta, IL-4, and IL-6 between smokers and non-smokers with different periodontal conditions? Do these biomarkers correlate with the severity and grade of periodontal disease?

Researchers will compare the saliva samples from smokers and non-smokers across the different periodontal conditions to see if there are significant differences in the biomarker levels. Participants will:

Provide saliva samples. Be categorized based on their smoking status and periodontal condition.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The periodontitis groups (Non-smoking and smoking) in the study will include systemically healthy patients who are clinically diagnosed with Stage II and III, generalized, Grade B, C periodontitis based on the consensus report of the 2017 World Workshop on Classification of Periodontal and Peri-Implant Diseases and Conditions.
  • Agreeing to participate in the study

Exclusion criteria

  • use of oral contraceptive drugs
  • use of antibiotics, immunosuppressants, or drug therapies in the last 6 months before the study;
  • history of excessive alcohol use;
  • pregnancy or breastfeeding status;
  • periodontal treatment during the last 6 months before the study.
  • Not agreeing to participate in the study
  • Not meeting the inclusion criteria

Trial design

100 participants in 4 patient groups

non-smoking - periodontally healthy
Description:
participants who reported never smoking and periodontal healthy.
Treatment:
Diagnostic Test: Clinical Measurements and Saliva Sample Collection
smoking - periodontally healthy
Description:
participants who reported smoking \>10 cigarettes per day and periodontal healthy.
Treatment:
Diagnostic Test: Clinical Measurements and Saliva Sample Collection
non-smoking - periodontitis
Description:
participants who reported never smoking, with clinical attachment loss ≥3 mm in \>30% of sites, with probing depth ≥5 mm in at least six teeth, and with radiographic bone loss extending to or beyond the middle third of the root in the coronal third will be included.
Treatment:
Diagnostic Test: Clinical Measurements and Saliva Sample Collection
smoking - periodontitis
Description:
participants who reported smoking \>10 cigarettes per day for \>5 years with clinical attachment loss ≥3 mm in \>30% of sites, with probing depth ≥5 mm in at least six teeth, and with radiographic bone loss extending to or beyond the middle third of the root in the coronal third will be included.
Treatment:
Diagnostic Test: Clinical Measurements and Saliva Sample Collection

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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