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Gingivitis clinical trials

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NCT ID: NCT00972803 Completed - Gingivitis Clinical Trials

The Effects of Pistacia Mutica on De Novo Dental Plaque Formation, Gingival Inflammation and Oral Microorganisms

Start date: May 2008
Phase: Phase 2
Study type: Interventional

Dental plaque is a well known etiologic factor for gingivitis. Recently, herbal extracts are a matter of scientific interest to inhibit plaque accumulation on teeth. The purpose of this study was to evaluate the effects of pistacia Mutica (PM) mouth wash on de novo dental plaque plaque formation, gingival inflammation indices and oral microorganisms.

NCT ID: NCT00964860 Completed - Gingivitis Clinical Trials

A Controlled Clinical Study to Determine the Gingivitis Benefit of Flossing

Start date: August 2009
Phase: Phase 3
Study type: Interventional

This is a randomized, controlled, examiner-blind, parallel group, four week clinical study comparing brushing plus flossing to brushing alone in 60 healthy adults with pre-existing gingivitis.

NCT ID: NCT00941668 Completed - Gingivitis Clinical Trials

Evaluate Inflammation Caused by Gingivitis in Adults

Start date: January 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the anti-inflammatory efficacy of a dentifrice

NCT ID: NCT00932347 Completed - Gingivitis Clinical Trials

Effect of Mouthwash Containing Camellia Sinensis Extracts on Oral Malodor

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine effect of Mouthwash containing Camellia sinensis extracts on oral malodor and gingival inflammation in gingivitis subjects.

NCT ID: NCT00926328 Completed - Gingivitis Clinical Trials

Comparative Efficacy of a Toothpaste That Reduces Plaque and Gingivitis

Start date: June 2007
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the performance of two toothpastes in controlling established gingivitis and dental plaque in adults.

NCT ID: NCT00885599 Completed - Gingivitis Clinical Trials

Efficacy of a Naturally-derived Mouthrinse for Gingival Inflammation

Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Gingivitis, defined as inflammation of the gingival tissues, has long been associated with bacterial accumulation [plaque] on the tooth surface adjacent to the gingiva, causing an inflammatory reaction. Experimental gingivitis in health adults can be induced by abstension from brushing teeth for 9 to 21 days, and can test the effects of numerous chemotherapeutic agents, rinses and toothpastes. Effective prevention of plaque accumulation can prevent destructive forms of periodontal disease. A recent link has been established between localized gingival inflammation and systemic inflammation and a number of disease processes. Periodontal disease may lead to elevated C-reactive protein [CRP], considered a potential risk factor for cardiovascular disease and stroke. It has been shown that reducing gingival inflammation is accompanied with a significant decrease in serum CRP levels. Naturopathic remedies for treating oral disease have been well documented in the medical and dental literature since early civilization, and have become more and more popular in recent years. We propose to study one such remedy, PERIORINSE. This remedy consists of a number of herbs, and has been shown to exhibit antibacterial and anti—inflammatory effects. Specifically, it has been shown to block the proteolytic effects seen in gingival inflammation . This study will evaluate the efficacy of this formulation, using currently accepted clinical testing protocols. A Random sample of 100 healthy volunteers who fulfill all inclusion criteria and no exclusion criteria, will be included in the study. Patients will randomly selected to one of 4 treatment groups: PERIORINSE (n=25), CPC (Cepacol) mouthwash (25 patients), Listerine mouthwash (n=25), and placebo (colored water) mouthrinse. Patients will be examined at baseline, and Gingival Index taken for all teeth. A blood specimen will be taken to measure CRP levels as well. Patients will be given a full dental prophylaxis which includes scaling and tooth polishing, and given rinsing instructions and reminded to cease all other oral hygiene methods including brushing, flossing, and rinsing with any other rinse for a period of 14 days. On day 14, patients will be re-examined and Gingival Index taken for all teeth. Patients will be given a full dental prophylaxis which includes scaling and tooth polishing and required to reinstitute their original oral hygiene regimen. CRP levels will be measured again, as well.

NCT ID: NCT00855933 Completed - Gingivitis Clinical Trials

A Controlled Clinical Study to Determine the Gingivitis Benefit of Flossing

Start date: January 2009
Phase: Phase 4
Study type: Interventional

This is a randomized, controlled, examiner-blind, parallel group, four week clinical study comparing brushing plus flossing to brushing alone in healthy adults with mild-to-moderate gingivitis.

NCT ID: NCT00779909 Completed - Gingivitis Clinical Trials

Dose-dependent Anti-inflammatory Effects of Vitamin D in a Human Gingivitis Model

Start date: December 2008
Phase: Early Phase 1
Study type: Interventional

The burden of chronic gingivitis and periodontitis in the US is disproportionately high among Non-Hispanic Blacks compared to Non-Hispanic Whites. Chronic gingivitis is a highly prevalent chronic inflammatory disease that may progress into periodontitis, a major cause of tooth loss, Data from in-vitro and animal studies suggest anti-inflammatory effects of vitamin D; however, if and over what dose-range vitamin D may have anti-inflammatory effects in humans is uncertain. Recent clinical studies indicate that beneficial effects of vitamin D for several important outcomes may occur over a wide range of serum 25-hydroxyvitamin D (25-OHD) concentrations, possibly up to concentrations that would require vitamin D intakes ranging from 2 to more than 10 ten times higher than the current RDA for vitamin D. Because dark skin pigmentation is a potent inhibitor of vitamin D photosynthesis, Non-Hispanic Blacks have much lower 25-OHD serum levels than Non-Hispanic Whites. These differences in vitamin D status may partially explain the racial disparities in prevalence of chronic gingivitis and periodontitis observed in the US. We hypothesize that oral cholecalciferol supplementation can reduce susceptibility to gingivitis over a wide range of serum 25-OHD concentrations in Non-Hispanic Whites and Non-Hispanic Blacks. We propose to conduct a simple, single-center, randomized, double-blind, placebo-controlled parallel-group dose-ranging study. We will compare placebo to doses of 500 IU, 2,500 IU and 5,000 IU vitamin D3 per day. We will compare the severity of gingival inflammation that develops in response to a 28-day period of unlimited plaque growth (experimental gingivitis) between dosage groups. Furthermore, we will evaluate the association between achieved 25-OHD levels and gingival inflammation. The results of this study will have several important implications, as dietary vitamin D supplementation may be a simple, safe and inexpensive means by which to reduce racial/ethnic disparities in gingivitis, as well as to reduce the overall burden of oral disease in the population as a whole. The study will elucidate the dose-response relationship of the anti-inflammatory effects of vitamin D, which in turn may lead to a revision of the current recommendations regarding nutritional supplementation of vitamin D in order to optimize the prevention of important medical conditions and diseases and reduce racial health disparities.

NCT ID: NCT00762528 Completed - Gingivitis Clinical Trials

Compare Anti-inflammatory Dentifrices

Start date: February 2009
Phase: Phase 4
Study type: Interventional

Plaque induced gingivitis

NCT ID: NCT00762515 Completed - Dental Plaque Clinical Trials

Clinical Study to Evaluate the Treatment of Gingivitis of Two Toothpastes

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The objective is to compare two commerical oral products for the treatment of gingivitis.