Skip to content

The Chromatic Evaluation of Universal Nano-hybrid Composites

The Chromatic Evaluation of Universal Nano-hybrid Composites

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06251921
Enrollment
30
Registered
2024-02-09
Start date
2024-01-23
Completion date
2025-03-31
Last updated
2024-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Lifestyle

Keywords

resin-based composite, color, pre-heated

Brief summary

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.

Detailed description

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.

Interventions

PROCEDURERestoration

with resin-based composite

Sponsors

Iuliu Hatieganu University of Medicine and Pharmacy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Clinical inspection of the restorations24 hoursThe blind observer will clinically inspect the restorations , following the Ryge scale criteria

Countries

Romania

Contacts

Primary ContactCorina Prodan, dr.
corinamirelaprodan@gmail.com0040946981859

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026