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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03727035
Other study ID # MADC/IRB-XV/2017/302
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 10, 2018
Est. completion date December 15, 2019

Study information

Verified date October 2019
Source Meenakshi Ammal Dental College and Hospital
Contact Jaideep Mahendra, MDS;PhD
Phone 9444963973
Email jaideep_m_23@yahoo.co.in
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The quantification of CD163 will be analysed in the subgingival plaque samples of generalized chronic periodontitis patients with and without diabetes mellitus. The demographic and the periodontal parameters were assessed and the correlated with the quantification of the CD163. The CD163 gene expression was analyzed with RT-PCR and the quantification of CD163 will be done using ELISA.


Description:

The quantification of CD163 will be analysed in the subgingival plaque samples of generalized chronic periodontitis patients with and without diabetes mellitus. A total of 80 subjects with generalized chronic periodontitis were selected and divided into two groups. Group I comprised of 40 subjects who were diagnosed with generalized chronic periodontitis without any systemic conditions. Group II comprised of 40 generalized chronic periodontitis patients with type II diabetes mellitus. Demographic variables such as age, weight, height, BMI and income and the clinical parameters such as plaque index, bleeding on probing, probing pocket depth and clinical attachment level were recorded. Subgingival plaque samples were collected from both the groups.The collected samples were subjected to further molecular analysis for the CD163 expression using RT-PCR and for the CD163 quantification using ELISA. The elevated levels of CD163 in the subgingival plaque samples of generalized chronic periodontitis subjects with diabetes is expected and the early identification of patients at risk for diabetes mellitus and periodontitis.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date December 15, 2019
Est. primary completion date November 30, 2019
Accepts healthy volunteers
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria:

1. Patients willing to participate in the study.

2. Patients within the age group of 30-65 years (both male and female)

3. Patients should have = 10 natural teeth.

4. Criteria for selection of generalized chronic periodontitis:

- Patients having 30% or more sites with clinical attachment loss(CAL) = 5mm.

5. Criteria for selection of type II diabetes mellitus:

- Patients having HbA1C <7

Exclusion Criteria:

1. Patients with systemic conditions such as respiratory diseases, renal disease, liver disease, rheumatoid arthritis, allergy, advanced malignancies and HIV infection will be excluded from the present investigation.

2. Patients on drugs such as corticosteroids, antibiotics, aspirin, within 3months of investigation will be excluded.

3. Current smokers, individuals who quit smoking less than 6 months.

4. Patients who had undergone periodontal therapy within the previous 6 months.

5. Pregnant women (which may alter the oral flora).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
India Jaideep Mahendra Chennai Tamilnadu

Sponsors (1)

Lead Sponsor Collaborator
Meenakshi Ammal Dental College and Hospital

Country where clinical trial is conducted

India, 

References & Publications (1)

Detzen L, Chen SCY, Cheng B, Papapanou PN, Lalla E. Increased levels of soluble CD163 in periodontitis patients. J Clin Periodontol. 2017 Jun;44(6):585-590. doi: 10.1111/jcpe.12731. Epub 2017 May 16. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Expression of CD163 gene Expression of CD163 gene using RT-PCR 12 months
Secondary Quantify the levels of CD163 Quantify the levels of CD163 using ELISA 12 months
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