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Recruiting NCT07627295

Impact of Finishing/Polishing Systems on Ormocer VS Methacrylate Based Bulk Fill Flowable Composite in Class V

No phase Interventional Class V Restorations

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: one-step finishing and polishing system., two-step finishing and polishing system., three-step finishing and polishing system..
Who it may be relevant to
Registry conditions: Class V Restorations. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Impact of Finishing/Polishing Systems on Ormocer Versus Methacrylate Based Bulk Fill Flowable Composite in Class V Restorations: Clinical Study and Laboratory Investigations

Overview

The goal of this clinical trial is to evaluate and compare. Impact of finishing/polishing systems on ormocer versus methacrylate-based bulk-fill flowable composite in Class V restorations: The main question it aims to answer is the following: Are there any differences between finishing/polishing systems on Ormocer versus methacrylate-based bulk-fill flowable composite?

Detailed description

This study will evaluate the impact of three different finishing/polishing systems on ormocer versus methacrylate-based bulk-fill flowable composite in Class V restorations on adult patients' anterior teeth. First, investigators will use an ormocer and methacrylate-based bulk-fill flowable composite in Class V restorations in anterior teeth. Then each patient will receive three different finishing/polishing systems. Investigators will follow patients at 2 weeks, 6 months, 18 months, and 24 months to assess the restorations according to the FDI criteria as esthetic properties (A1 surface luster and surface texture; A2 marginal staining; A3 color match), functional (F1 fracture/retention; F2 marginal adaptation), and biological (B1 caries at restoration margin). The results will help dentists choose the most appropriate finishing/polishing systems for Class V restoration cases.

Interventions

  • Other one-step finishing and polishing system.
    • Each class V restoration will be restored with an ormocer-based bulk-fill flowable composite material or methacrylate-based restorative according to the manufacturer's instructions for use, and then each class V restoration will be subjected to a one-step finishing and polishing system.
  • Other two-step finishing and polishing system.
    Each class V restoration will be restored with an ormocer-based bulk-fill flowable composite material or methacrylate-based restorative according to the manufacturer's instructions for use, and then each class V restoration will be subjected to a two-step finishing and polishing system.
  • Other three-step finishing and polishing system.
    Each Class V restoration will be restored with an ormocer-based bulk-fill flowable composite material or methacrylate-based restorative according to the manufacturer's instructions for use, and then each Class V restoration will be subjected to a three-step finishing and polishing system.

Primary outcome measures

  • FDI criteria score-aesthetic properties (A1 surface luster and surface texture; A2 Marginal staining; A3 color match), Functional (F1 Fracture/Retention; F2 marginal adaptation), biological (B1 caries at restoration margin) [Time frame: Post-restoration baseline (2 weeks), 6, 12, 18, and 24 months]

Eligibility criteria

Inclusion criteria

  • Three pairs of buccal cervical supragingival carious lesions in anterior teeth
  • Complete and normal occlusion
  • Good oral hygiene
  • Willingness to attend follow-up and recall visits for 2 years

Exclusion criteria

  • Teeth requiring direct pulp capping
  • Poor oral hygiene or failure to complete the oral hygiene phase
  • Chronic periodontitis
  • Pulpitis or non-vital teeth
  • Current orthodontic treatment
  • Presence of parafunctional habits
  • Systemic diseases
  • Previous or ongoing bleaching procedures
  • Smoking patients

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Double blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of Dentistry, Mansoura University — Al Mansurah

Identifiers

NCT: NCT07627295 · MD250825

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗