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.

N/ANot Yet RecruitingNCT07432724

Cairo University50 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Diabetes Mellitus (DM)

Interventions

bioactive compositeOTHER

the bioactive component present in the composite restoration.

Eligibility

Sex: ALLMin age: 20 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Patients indicated for a Class I posterior composite restoration * permanent tooth * ICDAS 3 or 4 Exclusion Criteria: * uncontrolled diabetic patients * primary dentition * special needs

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

Central Contacts

Sara Mohamed Manaa, PhD

CONTACT

00201022484815 sara.mohamed.manaa@hotmail.com

yomna sayed, lecturer

CONTACT

00201006781076 yomna.sayed@dentistry.cu.edu.eg

Data from ClinicalTrials.gov

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