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Treatment of Residual Pockets in Periodontal Patients Using an Oscillating Chitosan Device

Treatment of Residual Pockets in Periodontal Patients Using an Oscillating Chitosan Device - A Randomized Parallel Arm Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06127069
Enrollment
36
Registered
2023-11-13
Start date
2021-09-08
Completion date
2022-11-29
Last updated
2023-11-18

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

Conditions

Periodontitis

Keywords

residual pockets, chitosan, treatment of periodontitis

Brief summary

The aim of the current study was to investigate the effect of a chitosan brush on the treatment of residual pockets in patients already treated for periodontal disease. Thirty-six patients with chronic periodontitis (Stage ΙΙΙ, ΙV) that had already completed causative therapy and exhibited at least two residual periodontal pockets ≥ 5mm that bled on probing, were randomly assigned to two groups. In the test group debridement of residual pockets was performed with ultrasonic scaler and the chitosan brush, whereas in the control group only ultrasonic scalers were used.

Interventions

debridement of periodontal pockets with ultrasonic scaler first and after with chitosan brush for 2 minutes

debridement of periodontal pockets only with ultrasonic scaler

Sponsors

Aristotle University Of Thessaloniki
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Intervention model description

randomized parallel arm clinical trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Subjects aged 18 or over * Subjects diagnosed with chronic periodontitis, Stage III or IV, and had received full mouth scaling and root planning at least three months prior to baseline examination * Subjects with at least two residual periodontal pockets of at least 5mm depth that bled on probing * Full mouth plaques scores ≤20%

Exclusion criteria

* Subjects that had received antibiotic therapy 6 months prior to initial examination * Subjects with compromised systemic conditions * Patients undergoing chemotherapy or radiotherapy * Pregnant or lactating women

Design outcomes

Primary

MeasureTime frameDescription
Probing Pocket Depthbaseline, 6 weeks, 3 months, 6 monthsthe distance from the mucosa margin to the bottom of the periodontal pocket
MMP-8baseline, 6 weeks, 3 months, 6 monthslevels of matrix metalloproteinase -8 in gingival crevicular fluid

Secondary

MeasureTime frameDescription
Bleeding on Probingbaseline, 6 weeks, 3 months, 6 monthspresence or absence of bleeding after probe insertion in the periodontal pocket
Clinical Attachment Levelbaseline, 6 weeks, 3 months, 6 monthsthe distance from cementoenamel junction to the bottom of periodontal pocket
Gingival Recessionbaseline, 6 weeks, 3 months, 6 monthsthe distance from cementoenamel junction to the mucosa margin

Countries

Greece

Outcome results

None listed

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