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Adjunctive Effect of Photodynamic Therapy on Halitosis

Adjunctive Effect of Photodynamic Therapy on Halitosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06764342
Enrollment
40
Registered
2025-01-08
Start date
2025-01-08
Completion date
2025-06-25
Last updated
2025-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Halitosis, Periodontitis

Keywords

halitosis, periodontitis, full-mouth disinfection, antimicrobial photodynamic therapy, real time polymerase chain reaction, bacteria

Brief summary

The present study aims to evaluate bad breath in patients undergoing gingival treatment combined with tongue scraping and laser and to assess its potential benefits for both periodontal and microbiological condition. Firs patients will be selected among those who participated in a privies study. Additional patients will be also invited. They must have gum disease and bad breath. Treatments will be completed within 24 hours and oral samples will be collected with thin paper points. Bad breath will be evaluated by a professional and a specific gas machine.

Detailed description

The present study aims to evaluate halitosis in patients undergoing non-surgical periodontal therapy \[(Full-mouth disinfection (FMD) combined with tongue scraping and antimicrobial photodynamic therapy (aPDT), and to assess its potential benefits for both periodontal and microbiological condition. A pilot study will be performed with participants who took part almost 10 years ago in the study NCT02368678. They will be invited by phone contact. In addition, new participants will be recruited by convenience in dental clinics from the Federal University of Minas Gerais until completion of 20 participants per group. Individuals with stage III periodontitis and halitosis (organoleptic method \> 2), will be allocated into two periodontal treatment groups. Halitosis will be assessed using the organoleptic method and gas chromatography (OralChroma device) at three time points: before and after treatments. Microbiological samples will be collected before and after treatments from periodontal pockets and pooled samples from the tongue dorsum. These samples will be analyzed by using real-time PCR (q-PCR) aiming at detecting target bacterial species.

Interventions

RADIATIONFull-mouth scaling combined with antimicrobial photodynamic therapy

After full-mouth scaling procedures antimicrobial photodynamic therapy was carried out using a laser-activated disinfection device with a red laser emission (wavelength: 630 nm, irradiance: 2000-4000 mW/cm², spot size at the probe tip: 8 mm diameter) and high-viscosity methylene blue gel (0.1 mg/mL) which was applied at six spots on the tongue dorsum. Antimicrobial photodynamic therapy was also applied iIn sites with altered periodontal pocket depth (≥ 4mm). The dye remained in the pockets for 10 minutes to ensure full absorption and its excess was rinsed with sterile saline after laser exposure.

PROCEDUREfull-mouth scaling

Full-mouth scaling within 24 hours, divided into two sessions of ultrasonic instrumentation followed by manual supra- and subgingival scaling and root planing. Tongue cleaning was performed with a tongue scraper.

Sponsors

Federal University of Minas Gerais
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* self-reported halitosis; * organoleptic score \>2; * stage III periodontitis; * at least 14 teeth.

Exclusion criteria

* smokers or former smokers; * individuals diagnosed with diabetes and/or immune diseases; * pregnant or lactating women; * individuals with removable partial dentures and/or fixed or removable orthodontic appliances; * systemic use of antibiotics or anti-inflammatory drugs in the last three months; - individuals who required prophylactic antibiotics for periodontal exams and treatments; * individuals who regularly used or had used any type of mouthwash in the past three months; * individuals who underwent periodontal treatment in the six months prior to the study.

Design outcomes

Primary

MeasureTime frameDescription
sulfur volatile compounds changesbaseline versus 21 and 45 days after treatmentpre and post-treatment changes in levels (parts per billion) of CH3SH, a sulfur volatile compound

Secondary

MeasureTime frameDescription
Changes in periodontal probing depthbaseline versus 45 days after treatmentPre and pos-treatment changes in periodontal pocket depth (mm)
Changes in organoleptic testingBaseline versus 45 days after treatmentPre and post-treatment changes in organoleptic scores
Changes in tongue total bacteria countbaseline versus 45 days after treatmentPre- and post-treatment changes in total bacteria counts from tongue dorsal samples

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026