Ultrasonic Scaler VS Erythritol for Peri-implant Maintenance of Loaded Implants With Crowns Made by Different Materials
NCT06496594 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2025-04-08
Summary
The aim of the study is to assess the effect of a 12-month peri-implant protocol with erythritol orultrasonic scaler with peek inserts for dental implants with crowns made by different materials .
Patients will be randomly divided into two groups:
Erythritol group: erythritol with a particle size of \~14 µm will be used for 5 seconds (AIRFLOW® PLUS EMS) Ultrasonic scaler group: a piezoelectric handpiece with peek inserts (Mini Piezon EMS; PI EMS) .
Different subgroups will be defined according to the material of the dental crown of the related implant.
The mechanical debridement appointments will be carried out at the baseline, after 6 months, and after 12 months, after instruction and motivation of the patient, completion of the clinical chart with the recording of the Probing Depth (evaluation in mm of the peri-implant sulcus taken by a periodontal probe; 4 surfaces of the gingival margin are detected: vestibular, palatal/lingual, mesial, distal), Bleeding on Probing and Plaque Control Record.
Conditions
- Peri-implant Mucositis
Interventions
- OTHER
-
Erythritol prophylactic powders
erythritol with particle size of \~14 µm will be used for 5 seconds (AIRFLOW® PLUS EMS)
- OTHER
-
Ultrasonic scaler with peek inserts
ultrasonic scaler, a piezoelectric handpiece with peek inserts (Mini Piezon EMS; PI, EMS) will be used.
Sponsors & Collaborators
-
University of Pavia
lead OTHER
Principal Investigators
-
Andrea Scribante · University of Pavia
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-03-30
- Primary Completion
- 2025-02-10
- Completion
- 2025-02-15
Countries
- Italy
Study Locations
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