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"Study of Halitosis in Patients With Advanced Chronic Periodontitis" (HACP)

F

Federal University of Minas Gerais

Status

Completed

Conditions

Periodontitis
Halitosis
Periodontal Disease

Treatments

Procedure: Scaling and Root Planning (SRP)
Procedure: Full Mouth Scaling (FMS)

Study type

Interventional

Funder types

Other

Identifiers

NCT02368678
K4gnj9dd

Details and patient eligibility

About

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

Full description

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.

Enrollment

30 patients

Sex

All

Ages

35 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Scaling and Root Planning (SRP)
Active Comparator group
Description:
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.
Treatment:
Procedure: Scaling and Root Planning (SRP)
Full Mouth Scaling (FMS)
Active Comparator group
Description:
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.
Treatment:
Procedure: Full Mouth Scaling (FMS)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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