Skip to content

Full Mouth Ultrasonic Debridement Carried Out Either by Piezoelectric or Magnetostrictive Device

Clinical and Patient Centred Outcome Performance of Full Mouth Ultrasonic Debridement Carried Out for the Treatment of Periodontitis Performed Either by Piezoelectric or Magnetostrictive Device. A Randomized Controlled Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05279950
Enrollment
52
Registered
2022-03-15
Start date
2022-04-10
Completion date
2022-10-30
Last updated
2022-03-15

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

Conditions

Periodontitis, Adult

Keywords

periodontitis, patient centred outcomes, magnetostrictive

Brief summary

Treatment of periodontitis requires removal of dental biofilm both through professional mechanical plaque removal and domiciliar oral hygiene procedures. This study aims to compare biometric and psychological results after professional treatment of periodontitis carried out by piezoelectric or magnetostrictive ultrasonic devices.

Detailed description

Patients diagnosed with periodontitis will be assessed for eligibility criteria. Full-mouth periodontal assessment will be performed by an examiner to detect severity and extension of the disease. Thereafter, patient will receive oral hygiene instruction and a closed envelope with patient allocation will be opened. After the allocation to the intervention group, full-mouth ultrasonic debridement will be delivered to the patient by an operator and information about patient perception will be collected. Three months later, patients will be recalled for a new periodontal assessment.

Interventions

the use of ultrasonic oscillating tips allows supragingival and subgingival biofilm and dental calculus removal

the use of ultrasonic oscillating tips allows supragingival and subgingival biofilm and dental calculus removal

Sponsors

University of Siena
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* \>18 years * periodontitis of stage 1 and 2 * absence of systemic chronic disease

Exclusion criteria

* anticoagulants treatment * antibiotic treatment 3 months before the screening visit

Design outcomes

Primary

MeasureTime frameDescription
Pain perceptionthrough study completition, 1 yearvas scale (0-10) for perception of pain after treatment
noisethrough study completition, 1 yearvas scale (0-10) for perception of noise after treatment
vibrationthrough study completition, 1 yearvas scale (0-10) for perception of vibration after treatment

Secondary

MeasureTime frameDescription
pocket closurethrough study completition, 1 yearchange of pocket probing depth (millimeter) after treatment measured with a periodontal probe

Countries

Italy

Contacts

Primary Contactnicola Discepoli
NDISCEPOLI@ME.COM3395256148
Backup ContactNicola Discepoli
ndiscepoli@me.com0039 3395256148

Outcome results

None listed

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