Viewing Study NCT06288919



Ignite Creation Date: 2024-05-06 @ 8:12 PM
Last Modification Date: 2024-10-26 @ 3:22 PM
Study NCT ID: NCT06288919
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-04-26
First Post: 2024-02-23

Brief Title: Erythritol vs Ultrasonic Scaler Prophylaxis Systems on Dental Implants With Crowns Made by Different Materials
Sponsor: University of Pavia
Organization: University of Pavia

Study Overview

Official Title: Erythritol vs Ultrasonic Scaler Prophylaxis Systems on Dental Implants With Different Types of Crowns Randomized Clinical Trial
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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 palatallingual mesial distal Bleeding on Probing and Plaque Index
Detailed Description: 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 feldspathic ceramic zirconia and lithium disilicate

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 palatallingual mesial distal Bleeding on Probing and Plaque Index

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None