Clinical Trial

Erythritol vs Ultrasonic Scaler Prophylaxis Systems on Dental Implants With Crowns Made by Different Materials

Active, Not Recruiting
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Record status
This record was last updated January 13, 2025 (before its estimated April 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
The aim of the study is to assess which prophylaxis methods is the most suitable for peri-implant hygiene between erythritol and ultrasonic scaler with peek inserts. A randomized clinical trial will be conducted on the patient. 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) will be used. Different subgroups will be defined according to the material of the dental crown of the related implant. The oral hygiene session will be carried out every 6 months (2-years follow-up; 6 sessions), 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 Index.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2024-02-29; most recent amendment 2025-01-09.
Status change: Enrolling by Invitation → Active, Not Recruiting 2025-01-09
Status change: Not Yet Recruiting → Enrolling by Invitation 2024-04-25
Trial Details
NCT Number NCT06288919
Lead Sponsor University of Pavia
Conditions Dental Implant Failed, Peri-implant Mucositis, Peri-Implantitis
Enrollment 120 participants
Start Date 2024-03-01
Primary Completion 2026-04-01 (estimated)
Study Completion 2026-04-10 (estimated)
Updated on ClinicalTrials.gov 2025-01-13