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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04426604
Other study ID # AMAI-CU-2020-06-07
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 21, 2020
Est. completion date September 2021

Study information

Verified date July 2021
Source Cairo University
Contact Aya Mohamed Adly Ibrahim, Master's Degree
Phone +201221528843
Email aya.mohamed@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will be conducted to evaluate the clinical performance and validity of both light-induced fluorescence intraoral camera and laser-induced fluorescence device in comparison to visual-tactile assessment method in detection of secondary caries around margins of resin composite restorations.


Description:

Each patient should have at least one resin composite restoration. The restoration will be evaluated by all diagnostic methods. Each examiner will independently record the dental findings using all methods, the visual- tactile assessment method and both fluorescent-aided identification methods. The visual-tactile assessment method includes the use of mirror, probe under good illumination condition, while the fluorescent-aided identification methods will be performed by both light-induced fluorescence intraoral camera and laser-induced fluorescence device. Then Diagnostic performance for caries detection was evaluated, assessing the validity of each diagnostic method in diagnosing secondary caries around margins of resin composite restorations


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date September 2021
Est. primary completion date September 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients should be over 18 years of age. - Patients should have an acceptable oral hygiene level. - Patients should have at least one resin composite restoration. Exclusion Criteria: - Patients with a compromised medical history. - Patients with active severe periodontal disease.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Light induced fluorescence intraoral camera
Each restoration margins will be assessed by Light induced fluorescence intraoral camera to assess its validity in diagnosing secondary caries around margins of resin composite restorations
Laser-induced fluorescence device
Each restoration margins will be assessed by Laser-induced fluorescence device to assess its validity in diagnosing secondary caries around margins of resin composite restorations
Visual-tactile assessment method according to FDI criteria
Each restoration margins will be assessed by visual-tactile assessment method which includes the use of mirror, probe under good illumination condition to assess its validity in diagnosing secondary caries around margins of resin composite restorations

Locations

Country Name City State
Egypt Faculty of Dentistry, Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Validity of Fluorescence-based Devices versus Visual-tactile method Diagnostic performance for caries detection was evaluated, assessing the validity of each diagnostic method in diagnosing secondary caries around margins of resin composite restorations in terms of sensitivity and specificity. Through study completion, an average of 5 months