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Clinical Effects and Metagenomic Analysis of Using an Air Polishing Device With Erythritol Powder Compared to Scaling and Root Planing in Periodontal Maintenance Therapy.

Clinical Effects and Metagenomic Analysis of Using an Air Polishing Device With Erythritol Powder Compared to Scaling and Root Planing in Periodontal Maintenance Therapy: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07344805
Enrollment
20
Registered
2026-01-15
Start date
2023-07-01
Completion date
2025-07-01
Last updated
2026-01-15

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

Conditions

Periodontitis

Keywords

periodontal maintenance, erythritol, powder air polishing

Brief summary

Periodontitis is a chronic, multifactorial disease primarily driven by the accumulation of bacterial deposits. Treatment involves the mechanical removal of the biofilm, traditionally performed by scaling and root planing (SRP). However, SRP is time-consuming and can cause irreversible damage to both hard and soft tissues as well as postoperative sensitivity. Consequently, adjunctive or alternative air-polishing devices have been developed. The objective of this study is to compare the clinical and microbiological efficacy of an erythritol-powder air-polishing device versus SRP in periodontal maintenance therapy.To evaluate patient-reported pain and treatment time for erythritol air-polishing versus SRP. A randomized clinical trial was designed and participants were randomly assigned to one of two groups: Intervention: Perio-Flow® (air + erythritol powder) and PIEZON PS®. Control: Ultrasonic debridement followed by SRP with Gracey curettes.At baseline and at six months, probing depth, clinical attachment level, and bleeding on probing were recorded. Saliva samples were collected to detect the most prevalent periodontal pathogens. Patient discomfort during treatment was measured by a visual analog scale, and procedure duration was timed.

Interventions

DEVICEAIRFLOW® Prophylaxis Master

Periodontal Maintenance with Erythritol Air Polisher in periodontal patients.

DEVICECavitron® ultrasonic scaler

Periodontal maintenance with ultrasonic scaler and manual curettes in periodontal patients.

Sponsors

Cardenal Herrera University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have received basic periodontal treatment between 3-6 months before the study.

Exclusion criteria

* Pregnant or breastfeeding patients. * Use of systemic antibiotics within 6 months prior to the study. * Patients who smoke more than 10 cigarettes/day. * Uncontrolled diabetic patients.

Design outcomes

Primary

MeasureTime frameDescription
Improvement of clinical periodontal parameter: clinical attachment levelsix monthsMeasurement of clinical attachment level in milimeters
Improvement of clinical periodontal parameter: probing depthsix monthsMeasurement of probing depth in milimeters
Improvement of clinical periodontal parameter: bleeding indexsix monthsMeasurement of bleeding index in percentage.

Secondary

MeasureTime frameDescription
Changes in periodontal microbiomeSix monthsWe will present the following analyses: * Overall and differential abundance * Comparative relative inter-group community structure differences The overall and differential abundance of taxa will be analyzed using Kruskal Wallis non-parametric test. FDR Benjamini-Hochberg correction will be used to correct for multiple comparisons. Differences in community structure between experimental and control groups will be tested using Permanova. Permdisp test will be used to identify location vs. dispersion effects . The threshold for significance for all analyses will be set at p ≤ 0.05. 'BiodiversityR' version 2.11-1, 'PMCMR' version 4.3 and 'vegan' version 2.5-5 packages of the R software package version 36.6.0 (www.R-project.org) will be used.

Other

MeasureTime frameDescription
Patient discomfortSix monthsMeasurement of patient discomfort during the treatment by Visual Analogue Scale (VAS) Questionnaire (from no pain (score 0) to maximum pain imaginable (score 7)).

Countries

Spain

Outcome results

None listed

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