The effect of non-surgical periodontal treatment on salivary and serum visfati
Not Applicable
- Conditions
- generalized modorate to severe chronic periodontitis.Chronic periodontitis
- Registration Number
- IRCT2012080510501N1
- Lead Sponsor
- vice-chancellor for research of Tabriz university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 18
Inclusion Criteria
individuals whit BMI 18-24.9 kg/m2; natural teeth =20; GI>1; moderate to severe chronic periodontitis in which at least 30% sites have CAL=3mm and PPD=5mm and radiographic signs of bone loss are present. Exclusion criteria: individuals with systemic diseases that can alter the course of periodontal disease; pregnancy or lactation; hypertension; aggressive periodontitis; history of using anti hyperlipidemia medication or antibiotic in the preceding 6 months; ongoing usage of NSAIDs; a smoking habit; or those who had received scaling and root planning in the preceding 6 months.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Serum visfatin. Timepoint: before intervention, one month after intervention. Method of measurement: Eliza kit.;Salivary visfatin. Timepoint: before intervention, one month after intervention. Method of measurement: Eliza kit.
- Secondary Outcome Measures
Name Time Method Gingival index. Timepoint: before intervention, one month after intervention. Method of measurement: gingival index score.;Clinical attachment level. Timepoint: before intervention, one month after intervention. Method of measurement: prob.;Clinical pocket depth. Timepoint: before intervention, one month after intervention. Method of measurement: prob.