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Halitosis clinical trials

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NCT ID: NCT03053882 Completed - Bad Breath Clinical Trials

Efficacy of Peppermint and Green Tea in Malodor

Start date: January 2015
Phase: N/A
Study type: Interventional

Background: Herbal remedies can have the role of prevention and control of bad breath Since in the previous studies, therapeutic and antibacterial effect of green tea and peppermint had been proven .we studied and compared the effects of green tea and peppermint mouthwashes on halitosis. Materials and Methods: This single-blind clinical trial study with cross over design total of 88 volunteer dental students who complained bad breath and had organoleptic score (>= 2) and higher average test scores were enrolled. The students were divided randomly into two groups Green Tea - Peppermint were assigned. Organoleptic test in the baseline, on the 7 day, 14 and 21 measured after rinsing the mouthwashes .As well as the satisfaction of both plants on the last day was considered. Data analysis was performed using tests; Wilcoxon signed rank test, Mann Whithney u, GEE (Generalized Estimating Equation -ordinal logistic regression).

NCT ID: NCT03031756 Completed - Halitosis Clinical Trials

Efficacy of Glycine Powder Air-Polishing Combined With Scaling and Root Planing in the Treatment of Periodontitis and Halitosis

Start date: January 2015
Phase: N/A
Study type: Interventional

The aim of this clinical study was to evaluate the clinical efficacy of using perio flow adjunctively with mechanical instrumentation on periodontal parameters and halitosis. Sixty patients who presented with 4-6-mm probing pocket depth (PPD) were recruited for the study. Patients were randomly assigned to glycine powder air-polishing (GPAP) or control groups. For both groups PPDscores were recorded at the baseline and 1 month. Volatile sulphur compound (VSC) values were measured by a halimeter at the baseline, immediately after treatment, and at 7 days, 14 days and 1 month.

NCT ID: NCT02794766 Completed - Halitosis Clinical Trials

Inulin and S. Salivarius Reduce Halitosis

Start date: March 2014
Phase: Phase 2
Study type: Interventional

Halitosis associated with tongue coating results from the production of volatile sulfur compounds by bacterial action. The use of prebiotics and probiotics might be useful in treating such condition. The aim of this study was to evaluate the effect of the prebiotic inulin combined with the probiotic Streptococcus salivarius (SS) on halitosis by coating.

NCT ID: NCT02692495 Completed - Clinical trials for Nutritional and Metabolic Diseases

Evaluation of Potential Screening Tools for Metabolic Body Odor and Halitosis

Start date: April 2009
Phase: N/A
Study type: Observational

This study is designed as a retrospective cohort study to evaluate the potential of diagnostic procedures in defining populations of patients self-reporting unexpected and uncontrollable episodes of body odor and/or halitosis. The cohort - generally healthy individuals who had underwent multiple diagnostic tests recommended by their physicians and had not been diagnosed with any known medical condition - expressed their interest in trying gastrointestinal and nutritional diagnostic tests offered by Biolab Medical Unit. Our retrospective analysis will determine if these tests were useful as potential screening tools for metabolic body odor and halitosis.

NCT ID: NCT02689297 Completed - Halitosis Clinical Trials

Three Different Oral Hygiene Regimes on Three Volatile Sulfur Compounds

Start date: September 2013
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the effect of various oral hygiene regimes on three volatile sulfur compounds.

NCT ID: NCT02628938 Completed - Halitosis Clinical Trials

Effect of Miswak and Miswak Extract on Oral Malodor

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The aim of this experiment is to investigate the effect of Miswak on oral malodor and to determine whether this effect -if present- is the result of the mechanical action of Miswak or the chemical effect of its extract

NCT ID: NCT02368678 Completed - Periodontitis Clinical Trials

"Study of Halitosis in Patients With Advanced Chronic Periodontitis"

HACP
Start date: April 2013
Phase: N/A
Study type: Interventional

The objective of this study was to evaluate whether short-term full mouth disinfection protocol could have a greater reduction in the levels of halitosis and volatile sulfur compound or not, when compared to quadrant-wise scaling and root planing

NCT ID: NCT02113137 Completed - Halitosis Clinical Trials

Oral Hygiene Procedures on Reduction of Oral Malodor

Start date: September 2013
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the effect of various oral hygiene procedures on reduction of oral malodor.

NCT ID: NCT01948349 Completed - Oral Hygiene Clinical Trials

Impact of Bracket Design and Oral Hygiene Maintenance on Halitosis in the Orthodontic Patient

Start date: October 2012
Phase: N/A
Study type: Interventional

The advantage of self-ligating brackets on periodontal health has yet to be determined. In addition, the utilization of tongue scraping as an adjunct to traditional oral hygiene measures has yet to be studied in orthodontic patients. The aim of this study is to evaluate the effect of bracket type on plaque accumulation and also the impact of the appliance on oral malodor. In addition, the effect of tongue scraping on halitosis will be studied in patients undergoing orthodontic treatment. We hypothesize that self-ligating brackets will harbor less plaque than normal brackets, that tongue scraping will significantly decrease halitosis in patients undergoing orthodontic treatment and that patients with self-ligating brackets will exhibit less halitosis as measured by halimeter.

NCT ID: NCT01388023 Completed - Gingivitis Clinical Trials

Day Long Prevention of Oral Malodor With a Palatal Patch (SmellX) Containing A Herbal Formula

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

In a previous study the prevention of halitosis by the herbal formula and delivery system (SmellX), were established both in vitro and clinicaly. The duration of relief was established as long as 8 hours. In this study the investigators intend examine the day long efficacy of SmellX.