The Chromatic Evaluation of Universal Nano-hybrid Composites

N/ARecruitingNCT06251921

Iuliu Hatieganu University of Medicine and Pharmacy30 enrolled

Overview

The goal of this clinical trial is to evaluate the preheating effect of a group shade resin-based composite. The evaluation will be done on Ryge criteria. The main question it aims to answer is if there is a difference in time between preheated and non-heated resin-based composites in the oral cavity. Participants will be given treatment for cavities class 2 on premolars and molar and will come for recall at 24h, 1 week, 6 weeks, 3 months, 6 months, and 1 year.

The participants in the study will be adult patients (over 18 years old). Each patient will receive 2 restorations on premolars or molars, class 2, and medium cavities. The restorations will be performed under isolation with rubber-dam, and restored with preheated or not-heated resin-based composite. The occlusion will be tested and they will be notified to come for recall in order to make the evaluation of the restorations.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Healthy Lifestyle

Interventions

RestorationPROCEDURE

with resin-based composite

Eligibility

Sex: ALLMin age: 18 YearsMax age: 90 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Permanent dentition * The OHI index = 0 * Non-smoking patient * The patient has a healthy diet * The patient has parafunction * The antagonist tooth is healthy / with direct restorations * The caries are situated on proximal surfaces on premolars, molars * The cavities have a medium depth Exclusion Criteria: * Temporary dentition * The OHI index \>= 1 * The patient is smoker * The patient has an unhealthy diet * The patient suffers from bruxism, clenching * The antagonist tooth has an indirect restoration * The caries are situated on canines or incisors * The cavities have a deep or shallow depth

Locations (1)

GlobalDent

Cluj-Napoca, Cluj, Romania

RECRUITING

Outcomes

Primary Outcomes

Clinical inspection of the restorations

The blind observer will clinically inspect the restorations , following the Ryge scale criteria

Time frame: 24 hours

Clinical inspection of the restorations

The blind observer will clinically inspect the restorations , following the Ryge scale criteria

Time frame: 1 week

Clinical inspection of the restorations

The blind observer will clinically inspect the restorations , following the Ryge scale criteria

Time frame: 6 weeks

Clinical inspection of the restorations

The blind observer will clinically inspect the restorations , following the Ryge scale criteria

Time frame: 1 year

Central Contacts

Corina Prodan, dr.

CONTACT

0040946981859 corinamirelaprodan@gmail.com

Data from ClinicalTrials.gov

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