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Periodontitis clinical trials

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NCT ID: NCT02283736 Active, not recruiting - Clinical trials for Chronic Periodontitis

Efficacy of Oral Probiotic Administration in Patients With Chronic Periodontitis

probiotic
Start date: June 2014
Phase: Phase 2
Study type: Interventional

The aim of this randomized placebo- controlled clinical trial is to evaluate the effects of Lactobacillus rhamnosus SP1- containing probiotic tablets as an adjunct to scaling and root planning (SRP). Material and methods: Thirty six chronic periodontitis patients will be recruited and monitored clinically, immunologically and microbiologically at baseline, 3 and 6 months after therapy. All patients will receive scaling and root planning and randomly will be assigned over an experimental (SRP + probiotic, n=18) or control (SRP + placebo, n=18) group. The tablets will be used once per day during 3 months.

NCT ID: NCT02283554 Completed - Periodontitis Clinical Trials

Platelet Rich Fibrin With 1% Metformin Gel for Treatment of Intrabony Defects

Start date: November 2013
Phase: Phase 2
Study type: Interventional

ABSTRACT: Background: Platelet-rich fibrin (PRF) is a second-generation platelet concentrate which releases various growth factors that promote tissue regeneration. Metformin (MF), a member of biguanide group has been shown to facilitate osteoblast differentiation and thus may exhibit a favourable effect on alveolar bone . Current study was designed to evaluate the combined efficacy of PRF and 1% MF gel with open flap debridement (OFD) in treatment of intrabony defects in chronic periodontitis (CP) subjects. Methods: One hundred and twenty subjects with single defects were categorized into four treatment groups: OFD alone, OFD with PRF, OFD with 1% MF and OFD + PRF+1% MF. Clinical parameters like site specific plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), relative attachment level (RAL) and gingival marginal level (GML) were recorded at baseline before surgery and 9 months post-operatively. Percentage radiographic intra-bony defect depth reduction was evaluated using computer-aided software at baseline and 9 months.

NCT ID: NCT02283515 Completed - Clinical trials for Chronic Periodontitis

Efficacy of Locally Delivred 1.2% Rosuvastatin Gel in Chronic Periodontitis

Start date: January 2014
Phase: Phase 2/Phase 3
Study type: Interventional

BACKGROUND: Chronic periodontitis (CP) is an inflammatory condition affecting tooth supporting tissues and alveolar bone that surround the tooth leading to formation of deepend gingival sulcus that is highly prone to pathologic changes, ultimately bone resorption and tooth loss. In the literature, several pharmacologic agents have been administration via local delivery route, directly into diseased sites affirming greater improvement in periodontal status. Therefore, present study was conducted to determine the clinical effectiveness of subgingivally delivered 1.2% Rosuvastatin gel incorporated into an methylcellulose vehicle for its controlled release into intrabony defect sites in adjunct to scaling and root planing for treatment of chronic periodontitis patients. MATERIAL AND METHODS: Sixty five patients were categorized into two treatment groups: group I -SRP plus RSV, 1.2 mg and group II -SRP plus placebo. Clinical parameters included modified sulcus bleeding index (mSBI), probing depth (PD), and clinical attachment level (CAL), were recorded at baseline before SRP and at 1, 3, 4, and 6 months. Radiologic assessment of intrabony defect (IBD) fill was analysed at baseline and after 6months using computer-aided software.

NCT ID: NCT02282800 Completed - Clinical trials for Aggressive Periodontitis

Immunolocalization of 1,25,Dihydroxyvitamin D3 in Aggressive Periodontitis Patients

IVDAP
Start date: November 2010
Phase: N/A
Study type: Observational

The study was to intended to visualize the nuclear localization of vitamin D receptor in oral tissues of aggressive periodontitis patients to better understand the potential for receptor in disease activity or progression.

NCT ID: NCT02280122 Completed - Clinical trials for Generalized Chronic Periodontitis

Activated MMP-8 as Diagnostic Test for Periodontitis

MMP-8
Start date: September 2012
Phase: N/A
Study type: Observational

Background: Untreated periodontal disease may influence general health. However, how may a physician who is not trained in periodontal probing detect untreated periodontitis? Activated matrix metalloproteinase-8 (aMMP-8) in saliva correlates with periodontal probing parameters. Thus, sensitivity and specificity of a chair-side test for activated matrix metalloproteinase-8 to detect periodontitis was evaluated. Methods: Thirty cases (untreated chronic periodontitis; 15 generalized moderate and 15 generalized severe) and 30 controls (probing pocket depths ≤ 3 mm, vertical probing attachment level ≤ 2 mm at < 30% of sites) were examined periodontally. Further, the activated matrix metalloproteinase-8 test was performed. The test kit becomes positive with ≥ 25 ng/ml activated matrix metalloproteinase-8 in the sample.

NCT ID: NCT02274090 Completed - Periodontitis Clinical Trials

1% Metformin in Moderate and Severe Periodontitis

Start date: November 2013
Phase: Phase 2/Phase 3
Study type: Interventional

This study evaluates the efficacy of 1% Metformin gel in treatment of moderate and severe periodontitis subject.

NCT ID: NCT02273128 Completed - Osteoporosis Clinical Trials

A Study to Assess the Disturbances in Calcitonin Gene in Patients With Gum Disease and Osteoporosis

CTROP
Start date: June 2014
Phase: N/A
Study type: Observational

Osteoporosis and Periodontitis are multifactorial diseases which share common risk factors.The aim of the present study is to ellucidate polymorphisms in Calcitonin receptor gene? in patients with Osteoporosis and Periodontitis.

NCT ID: NCT02271815 Completed - Periodontitis Clinical Trials

A Clinical and Imaging Study to Evaluate a Novel Dentifrice

Start date: October 2014
Phase:
Study type: Observational

There is a need for toothpastes that more effectively remove oral biofilm, inhibit biofilm re-formation and support periodontal health. This is particularly important for patients with long-term orthodontic fixtures or prosthodontic appliances, and also for debilitated, diabetic and immunocompromised patients. The objective of this study is to evaluate the effects of toothpastes on plaque presence and removal, gingival and periodontal health, dental hard tissue mineralization, erosion, abrasion, and microstructure as well as dry/sore mouth. In addition to clinical scoring and photographs, tooth and gum sensitivity, saliva volume, pH and buffering and enamel health may be evaluated using tooth samples worn on removable dental retainers. These samples will be examined outside of the mouth using advanced optical techniques such as Optical Coherence Tomography (OCT), Fluorescence, various forms of microscopy and spectroscopy.

NCT ID: NCT02267239 Recruiting - Periodontitis Clinical Trials

Methodology Antiseptic Application, Influence on Oral Biofilm.

Start date: October 2014
Phase: Phase 4
Study type: Interventional

The study has the objective to compare two different methodology of application the antiseptic on the oral biofilm will be formed during 48h in situ on a specific device. The first one using the immersion in the antiseptic solution, as much of the authors did in the past. And the second way doing a active mouthwash, as the manufacturer recommends. The study will compare two different antiseptic solutions, the chlorhexidine (0.2% Oraldine Perio) and the essential oils (Listerine Mentol) with the two different application and compared the bacterial vitality, thickness and covering grade between solutions and with a basal sample.

NCT ID: NCT02248103 Completed - Clinical trials for Chronic Periodontitis

Comparison of Autogenous Periosteal Pedicle Graft and Collagen Membrane in Management of Periodontal Intrabony Defects

Start date: March 2013
Phase: N/A
Study type: Interventional

A clinical and radiographic evaluation of autogenous periosteal pedicle graft in comparison with collagen membrane for management of periodontal intrabony defects.