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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02775266
Other study ID # 00159
Secondary ID
Status Completed
Phase N/A
First received May 5, 2016
Last updated March 10, 2017
Start date February 2016
Est. completion date October 2016

Study information

Verified date March 2017
Source Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the effectiveness of non surgical periodontal therapy in addition to antioxidant(ALA) on resistin levels in patients with type 2 diabetes and periodontal disease


Description:

A total of 40 patients with diabetes and chronic periodontitis attending the department of periodontics will be recruited in the study. 40 subjects will be randomly divided into two groups(control group and test group with 20 subjects in each group). Clinical parameters such as gingival index, periodontal index, random blood sugar levels(RBS) and glycosylated hemoglobin levels (Hb1aC) will be recorded at baseline and after 3 months and 2ml of blood sample will be collected by venepuncture ( baseline and after 3 months) and stored in Ethylenediaminetetraacetic acid containing vials to identify the levels of resistin in the patients by Enzyme linked immunosorbent assay. Group A will receive Alpha lipoic acid at baseline for a period of 3 months. Both the groups will receive scaling and rootplaning at baseline.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 2016
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender All
Age group 35 Years to 60 Years
Eligibility Inclusion Criteria: Diabetic patients with Chronic periodontitis.

Exclusion Criteria: Smokers, Pregnant & lactating women, Prior periodontal therapy within 3 months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Alpha lipoic acid
Scaling and root planing will be done at baseline and systemic antioxidant Alpha lipoic acid 1800mg/day in 3 divided doses for a period of 3 months.
Procedure:
Scaling and Root planing
Scaling and root planing will be done at baseline.

Locations

Country Name City State
India Mohans Diabetic Centre Hyderabad Telangana

Sponsors (1)

Lead Sponsor Collaborator
Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre

Country where clinical trial is conducted

India, 

References & Publications (2)

Mealey BL, Oates TW; American Academy of Periodontology.. Diabetes mellitus and periodontal diseases. J Periodontol. 2006 Aug;77(8):1289-303. Review. — View Citation

Pendyala G, Thomas B, Kumari S. The challenge of antioxidants to free radicals in periodontitis. J Indian Soc Periodontol. 2008 Sep;12(3):79-83. doi: 10.4103/0972-124X.44100. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Serum Resistin Levels and HBAIC Levels 2ml of blood sample will be collected by venepuncture at baseline and after 3 months and will be assessed by ELISA stored in EDTA containing vials to identify the levels of resistin in the patients by ELISA.
Glycosylated hemoglobin levels (Hb1aC) will be recorded at baseline and after 3 months and assessed by Spectrophotometer.
3 months
Secondary Gingival Index Gingival index was recorded with william's periodontal probe at baseline and after 3 months 3 months
Secondary Probing pocket depth Were recorded with william's periodontal probe at baseline and after 3 months 3 months
Secondary Clinical Attachment levels Were recorded with william's periodontal probe at baseline and after 3 months 3 Months
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