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Expression of Trefoil Factors and Adrenomedullin in Subjects With Chronic Periodontitis and Coronary Heart Disease

M

Meenakshi Ammal Dental College and Hospital

Status

Unknown

Conditions

Coronary Heart Disease
Periodontal Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT04127474
MADC/IRB-XXIX/2019/468

Details and patient eligibility

About

To assess the demographic variables, periodontal parameters and to determine the expression of Trefoil factors 2 and 3 and Adrenomedullin in unstimulated saliva samples of periodontally healthy subjects with coronary heart disease and generalised chronic periodontitis subjects with and without coronary heart disease.

Full description

A total of 75 subjects will be recruited for the study based on the power of the study.

The selected subjects will be divided into 3 groups based on inclusion and exclusion criteria.

GROUP I:25Generalized chronic periodontitis subjects without coronary heart disease.

GROUP II: 25Generalized chronic periodontitis subjects diagnosed with coronary heart disease.

GROUP III: 25Periodontally healthy subjects diagnosed with coronary heart disease.

Demographic variables, periodontal parameters and biochemical parameters will be measured in all three groups

Enrollment

75 estimated patients

Sex

All

Ages

30 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Patients willing to participate in the study.

  2. Patients within the age group of 30-65 years.

  3. Patients should have ≥ 20 remaining natural teeth.

  4. For Group I

    • Systemically healthy, Generalized chronic periodontitis subjects with 30% or more sites with clinical attachment loss (CAL) ≥ 2mm, radiographic evidence of alveolar crestal bone loss ≥ 2mm from the cemento-enamel junction.

  5. For Group II

    • Generalized chronic periodontitis subjects with 30% or more sites with clinical attachment loss (CAL) ≥ 2mm, radiographic evidence of alveolar crestal bone loss ≥ 2mm from the cemento-enamel junction along with coronary heart disease.

  6. For Group III • Periodontally healthy subjects with Probing pocket depth (PD) less than 4mm, bleeding on probing (BOP) at ≤15% of tooth sites, no periodontal treatment (Scaling and root planing or periodontal surgery) within the previous 6 months and without evident clinical signs of gingival inflammation along with the presence of coronary heart disease.

Exclusion criteria

  1. Subjects with systemic conditions such as type I and type II diabetes mellitus, respiratory diseases, renal disease, liver disease, rheumatoid arthritis, allergy, advanced malignancies and HIV infection will be excluded from the present investigation.
  2. For Group I, subjects on drugs such as corticosteroids, antibiotics, within 6 months of investigation will be excluded.
  3. Current smokers and individuals who quit smoking less than 6 months.
  4. Patients who have undergone periodontal therapy within the previous 6 months.
  5. Pregnant women (pregnancy may alter the oral flora)

Trial design

75 participants in 3 patient groups

Group I
Description:
25 Generalized chronic periodontitis subjects without coronary heart disease.
Group II
Description:
25 Generalized chronic periodontitis subjects diagnosed with coronary heart disease.
Group III
Description:
25 Periodontally healthy subjects diagnosed with coronary heart disease.

Trial contacts and locations

1

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Central trial contact

Sruthi Srinivasan, BDS; Jaideep Mahendra, MDS, PhD

Data sourced from clinicaltrials.gov

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