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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03558113
Other study ID # CEBD-CU-2018-06-04
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 2018
Est. completion date November 2018

Study information

Verified date June 2018
Source Cairo University
Contact Haneen elmoselhy, master
Phone 01003778829
Email noonyelmoselhy@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 29
Est. completion date November 2018
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Exclusion Criteria:

Patients with a compromised medical history. Severe or active periodontal disease. Heavy bruxism or a traumatic occlusion.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
light induced fluorescence intraoral camera
intraoral oral light induced fluorescence diagnostic camera

Locations

Country Name City State
Egypt 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 reliability and reproducibility of intra oral light fluorescence camera using kappa strength in secondary craies diagnosis around composite restorations 6 months
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