Viewing Study NCT06425536



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06425536
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-06-26
First Post: 2024-05-17

Brief Title: Efficacy of Remineralizing Products Used in Molar Grooves Evaluation With Diagnodent Pen and Diagnocam
Sponsor: University of Pavia
Organization: University of Pavia

Study Overview

Official Title: Efficacy of Remineralizing Products Used in Molar Grooves RCT With Evaluation With Diagnodent Pen and Diagnocam
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-06
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: To evaluate the efficacy of enamel remineralization by biomimetic hydroxyapatite contained in microRepair-based Biorepair Total Protection toothpaste compared to the use of Bio Enamel Caries and Erosion toothpaste based on Fluoro-Hydroxyapatite and BioActive Complex evaluated with Diagnodent Pen and Diagnocam
Detailed Description: The recruited patients will be divided into

Group 1 Active group 20 patients undergoing quarterly oral hygiene sessions and home treatment using Biorepair Total Protection toothpaste 2 timesday

Gruppo 2 Active group 20 patients undergoing quarterly oral hygiene sessions and home treatment using Curasept Biosmalto Caries and Erosion toothpaste 2 timesday

For both groups Diagnodent Pen will be used to evaluate the degree of demineralization while Diagnocam will be used as qualitative evaluation

Other clinical indices to be collected are plaque index PI bleeding index BOP basic erosive wear examination BEWE Schiff Air Index SAI

The time frames of the study are

T0 baseline
T1 after 1 month
T2 after 3 months
T3 after 6 months

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