This Study is Conducted to Evaluate the 18-month Clinical Performance of Complete Bioactive Restorative System for Occlusal Restorations Between Diabetic and Non-diabetic Patients.

ConditionDiabetes Mellitus (DM)

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age20+

SponsorCairo University

About this trial

This study is conducted to evaluate the 18-month clinical performance of complete bioactive restorative system for occlusal restorations between diabetic and non-diabetic patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients indicated for a Class I posterior composite restoration

permanent tooth

ICDAS 3 or 4

Disqualifiers

uncontrolled diabetic patients

primary dentition

special needs

Trial design

Design model

Parallel

Treatments tested in this trial

bioactive composite
Other intervention
the bioactive component present in the composite restoration.

Treatment groups

50 Participants

are divided into 2 treatment groups

Group A: diabetic patientsExperimental treatment 1 intervention

Group B: Non diabetic patientsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Marginal discoloration

Measuring device: Modified USPHS criteria

Time frame

T0: Baseline T1: 6 months T2: 12 months T3: 18 month

Secondary outcomes

Marginal adaptation, color match, secondary caries, Retention, wear, and postoperative sensitivity.

measuring device: Modified USPHS criteria

Time frame

T0: baseline T1: 6 months T2: 12 months T3: 18 months

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Cairo University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: