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Reliability of Fluorescent Camera in Diagnosis of Occlusal Carious Lesion

Reliability of Fluorescent Camera and Caries Detection Dye Versus Visual- Assessment in Diagnosis of Occlusal Carious Lesion in Adult Patients: Invivo Diagnostic Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03224962
Enrollment
43
Registered
2017-07-21
Start date
2017-08-31
Completion date
2018-03-31
Last updated
2017-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caries

Keywords

pit and fissure caries

Brief summary

This study will be conducted to compare the diagnostic predictive values of a light induced fluorescence camera and Caries detection dye versus visual assessment method in identification of occlusal carious lesion.

Detailed description

A total of 43 volunteer patients will be assigned in this study. Each patient must have at least two occlusal carious lesions. Each lesion will be evaluated by three diagnostic methods (D), where D1 represents light induced fluorescence camera, D2 represents Caries detection dye. And D3 represents visual assessment method (ICDAS criteria)

Interventions

DEVICEfluorescence camera

drug - diagnostic test

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients should be over 18 Years old * Patient should have good oral hygiene and general health * patients With at least 2 non-cavitated first and/or second molar teeth in each quadrant of maxilla or mandible

Exclusion criteria

* Known allergy to any component of the dyes used. * Patients having caries at proximal, buccal, lingual surface. * Previously placed sealants or restorations. * Bruxism or malocclusion

Design outcomes

Primary

MeasureTime frameDescription
Reliability and level of agreement between operators for all diagnostic methods.3 monthsIt will be assessed using reliability & reproducibility by kappa strength measuring unit

Contacts

Primary Contactshimaa M Zenhom Abd El Rahman, B A
shimaa-maher@dentistry.cu.edu.eg(002)01001036094
Backup Contactamir hafez, lecturer
amir.hafez@dentistry.cu.edu.eg(002)01100001278

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026