Dietary Supplementation With Low-Dose Omega-3 Reduces Salivary TNF-α Levels in Patients With Chronic Periodontitis
- Conditions
- Chronic Periodontitis
- Registration Number
- NCT02719587
- Lead Sponsor
- İlker KESKINER
- Brief Summary
The investigators primary objective in this clinical intervention study, therefore, was to explore the impact of omega-3 PUFAs in conjunction with scaling and root planing on salivary markers (in patients with chronic periodontitis.
- Detailed Description
Thirty systemically healthy subjects with chronic periodontitis were enrolled and randomly allocated into two groups. The control group (n=15) was treated with scaling and root planing (SRP)+placebo whereas the test group (n=15) was treated with SRP and dietary supplementation of low-dose omega-3 PUFAs (6.25 mg EPA and 19.19 mg DHA). Clinical parameters were taken at baseline, 1, 3 and 6 months following therapy. Saliva samples were obtained at the same time intervals and analyzed for tumor necrosis factor-α (TNF-α) and superoxide dismutase (SOD).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- patients diagnosed with chronic periodontitis
- had at least nine posterior teeth (not including third molars and teeth with bridges and crowns)
- with 5-7 mm pocket depth
- three teeth with 6 mm or more of probing attachment loss enrolled in the study
- patients were excluded on the basis of periodontal surgery within the last year;
- SRP as part of initial periodontal therapy within the past 6 months;
- history of diabetes, any diseases or disorders that compromise wound healing, any history of acute or chronic inflammatory disease,
- any oral mucosal inflammatory condition (e.g., aphthous, lichen planus, leukoplakia, and oral cancer) and use of aspirin
- other non-steroidal anti-inflammatory drugs or antibiotics within the last 6 months.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method change in levels of salivary TNF alpha From baseline to 1, 3, 6 months
- Secondary Outcome Measures
Name Time Method change in levels of salivary SOD From baseline to 1, 3, 6 months