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"Study of Halitosis in Patients With Advanced Chronic Periodontitis"

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EstadoTerminado
Patrocinadores
Federal University of Minas Gerais

Palabras clave

Abstracto

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

Descripción

In recent years, several studies have shown that the levels of volatile sulfur compounds are higher in periodontitis patients. However, the relationship between periodontal disease and bad breath is still controversial. Aspects that should be clarified include its relation to periodontitis severity, the influence of risk variables and the subject of the present research, that is treatment choice. To help clinicians and patients when deciding about mechanical periodontal therapy, 30 patients with advanced chronic periodontitis were selected from the periodontics clinic, Dental School, Pontiphical Catholic University of Minas Gerais from April 2013 to May 2014. A complete periodontal clinical examination was performed and the following parameters were recorded: probing depth (PD), clinical attachment level (CAL), bleeding on probing, plaque index, and tongue coating index. Halitosis was assessed by using the organoleptic method and measurements of volatile sulfur compounds (VSC), including hydrogen sulfide (H2S) and methyl mercaptan (CH3SH) by using gas chromatography, at baseline and 90 days after non-surgical periodontal treatment. After periodontal clinical examination, individuals were randomly allocated to full-mouth scaling (FMS) - completed within 24 hours - or to conventional quadrant-wise scaling and root planing (SRP) - completed within 2 months. Halitosis and sulfur gas levels were were statistically compared (Mann-Whitney and Wilcoxon tests, p < 0.05). For inter- and intra-group comparisons regarding categorical variables Chi-square, McNemar, and Fisher exact tests were used. Primary outcome was halitosis changing.

fechas

Verificado por última vez: 01/31/2015
Primero enviado: 02/07/2015
Inscripción estimada enviada: 02/19/2015
Publicado por primera vez: 02/22/2015
Última actualización enviada: 02/19/2015
Última actualización publicada: 02/22/2015
Fecha de inicio real del estudio: 03/31/2013
Fecha estimada de finalización primaria: 04/30/2014
Fecha estimada de finalización del estudio: 04/30/2014

Condición o enfermedad

Periodontal Disease
Halitosis
Periodontitis

Intervención / tratamiento

Procedure: Scaling and Root Planning (SRP)

Procedure: Full Mouth Scaling (FMS)

Fase

-

Grupos de brazos

BrazoIntervención / tratamiento
Active Comparator: Scaling and Root Planning (SRP)
Scaling and root planing (SRP) (n=15): the traditional mechanical periodontal therapy consisting of quadrant-wise (30 min. per quadrant) scaling and root planning performed at weekly sessions (one or two weeks of interval between session) and completed within 2 months.
Procedure: Scaling and Root Planning (SRP)
Scaling and Root Planing (n=15): quadrant-wise scaling and root planing performed within four weekly session (30 min. per quadrant). Oral malodor was measured by organoleptic test and Oral Chroma (Abilit, Osaka Japan) prior to the oral examination, at Baseline and also at 90 days after treatment. Clinical monitoring and tongue coating index were taken at these same times. Oral hygiene instructions were given to all participants.
Active Comparator: Full Mouth Scaling (FMS)
Full mouth scaling (FMS) (n=15): the alternative mechanical periodontal therapy consisting of full-mouth scaling and root planning completed in a single stage within 24 hours; i.e two sessions (60 min. per session) in two consecutive days.
Procedure: Full Mouth Scaling (FMS)
Full Mouth Scaling (n=15): scaling and root planning was performed in a single stage (within 24 hours); two sessions (60 min. per session) in two consecutive days. Oral malodor was measured by organoleptic test and Oral Chroma (Abilit, Osaka Japan) prior to the oral examination, at Baseline and also at 90 days after treatment. Clinical monitoring and tongue coating index were taken at these same times. Oral hygiene instructions were given to all participants.

Criterio de elegibilidad

Edades elegibles para estudiar 35 Years A 35 Years
Sexos elegibles para estudiarAll
Acepta voluntarios saludablessi
Criterios

Inclusion Criteria:

- age between 35 and 60 years

- presence of at least 20 natural teeth

- diagnosis of chronic periodontitis

- halitosis

- no smokers

Exclusion Criteria:

- smokers or former smokers

- individuals diagnosed with diabetes and / or immunological disorders

- pregnant or lactating / patients with removable partial dentures and / or fixed or removable orthodontic appliance

- systemic use of antibiotics or anti-inflammatory in the last six months

- need for prophylactic use of antibiotics for performing the treatment

- regular use or use in the last six months of any kind of mouthwash

- individuals who underwent periodontal treatment in the 6 months preceding the start of the study

Salir

Medidas de resultado primarias

1. Change from baseline in Halitosis at 3 months [Baseline and 90 days]

Reduction in the number of patients with halitosis and improvement regarding halitosis severity

Medidas de resultado secundarias

1. Change from baseline in clinical attachment level at 3 months [Baseline and 90 days]

Gain of clinical attachment levels (mean values)

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