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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02537327
Other study ID # S56046
Secondary ID
Status Completed
Phase N/A
First received August 19, 2015
Last updated November 22, 2016
Start date August 2014
Est. completion date June 2016

Study information

Verified date June 2016
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Observational

Clinical Trial Summary

The aim of this study is to determine the incidence of recurrent caries around the different types of restorative materials (composites, amalgam, ceramics, crowns, etc.) and to better characterize recurrent caries lesions in terms of location and size of the lesions and type, material and age of the restoration.


Description:

The data will be collected from patients who are visiting the dental clinic for a check-up. These data will be retrieved in the patient records. In particular the clinical (mouth) exam and the radiographic images ('RX-bite-wings'), which are routinely taken during these check-up consultations, will be used for the evaluation of recurrent caries. Information regarding medical background, oral hygiene, sugar eating habits and possible parafunctional activities will also be gathered from the patient files. In addition, caries risk of the patients will be assessed using commercial kits for analysis of their saliva (Saliva-Check Buffer, GC, Tokyo, Japan) and dental plaque (Tri Plaque ID Gel, GC, Tokyo, Japan), which are a part of the routine care of the patients at the clinic.


Recruitment information / eligibility

Status Completed
Enrollment 450
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients visiting the university dental clinic (Department of Oral Health Care) for a dental check-up

Exclusion Criteria:

- Patients for who not all necessary data could be registered (incomplete mouth exam records, missing RX-bite wings, etc)

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium KU Leuven and UZ Leuven, Department of oral health sciences Leuven

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of recurrent caries Number of recurrent caries lesions (new caries lesion next to restoration) within a specified time period divided by the total number of restorations. Two years No
Secondary Caries risk of the patient Caries risk of each patient will be assessed based on scoring of several parameters such as: number of new caries lesions in the last 3 years (from patients' files), presence of relevant systemic disease (from patients' files), sugar consumption (from patients' files), oral hygiene (from patients' files) and results of the Saliva-check test and Tri plaque ID test. Two years No
See also
  Status Clinical Trial Phase
Recruiting NCT05696431 - Clinical Performance of Three Universal Adhesives in Posterior Restorations N/A