Reliability of Secondary Caries Detection Around Composite Restoration Using Light Induced Fluorescence

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

29 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-08-31

Study Completion Date

2018-11-30

Brief Summary

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A total of 29 volunteer patients will be assigned in this study. Each patient should have one resin composite restoration. The restoration will be evaluated by two diagnostic methods (D), where D1 represents visual-tactile assessment method (modified USPHS) and D2 represents light induced fluorescence intraoral camera

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Detailed Description

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Three operators, the researcher and the 2 supervisors, from the Conservative Dentistry Department, Faculty of Dentistry, Cairo University, will be the examiners in this study. Each examiner will record the dental findings using both the visual- tactile assessment method and the fluorescent-aided identification method. The visual-tactile assessment method includes the use of mirror, probe under good illumination condition, while the fluorescent-aided identification method will be performed by light induced fluorescence intraoral camera

Conditions

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Secondary Caries

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Screening of patients that come to the conservative dentistry department seeking dental care will continue until the target population is achieved. The patients' restorations will be subjected to visual examination and diagnosis using dental charts. Once the patients that are potentially eligible for this study are identified, they will be contacted by the research investigator who will explain the study and ascertains the patient's interest. If interested, more detailed evaluations and preparations are made.

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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visual tactile method

visual tactile method using the modified USHPS critiria

Group Type OTHER

light induced fluorescence intraoral camera

Intervention Type DIAGNOSTIC_TEST

intraoral oral light induced fluorescence diagnostic camera

Interventions

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light induced fluorescence intraoral camera

intraoral oral light induced fluorescence diagnostic camera

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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soprolife camera

Eligibility Criteria

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Inclusion Criteria

* Patients should be over 18 years of age. Patients should have an acceptable oral hygiene level. Patients must have at least one posterior resin composite restoration