Clinical Effectiveness of(VistaProof)in Comparison With ICDAS-II & Histological Validation for Detecting Occlusal Caries

Mohamed samy El-sayed

Status: Completed

Conditions: Light Fluorescence Device

Treatments: Procedure: fissurotomy; Device: vistacam proof; Other: ICDASII

Study type: Observational

Funder types: Other

Identifiers

NCT03940170

2222

Details and patient eligibility

About

a diagnostic accuracy study control trial is to be held to evaluate the Clinical performance of quantitative light fluorescence based device (Vistacam Proof) in comparison with the visual examination and histological validation in detection of initial pits and fissures caries

Enrollment: 24 patients

Sex: All

Ages: 15 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients aged from 15 to 50 years.
• Patient at least has one posterior pits and fissure occlusal caries.
• No gender restriction
• Co-operative patients who signed the informed consent.
• Good general health
• Acceptable oral health

Exclusion criteria

• Pregnancy.
• Disabilities.
• Systemic disease or severe medical complications.
• Allergic history concerning methacrylate.
• Rampant caries.

Trial design

24 participants in 3 patient groups

vistacam

Treatment:

Device: vistacam proof

ICDAS II

Treatment:

Other: ICDASII

Fissurotomy

Treatment:

Other: ICDASII

Procedure: fissurotomy

Device: vistacam proof