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Clinical Trials/NCT06032689
NCT06032689CompletedNot Applicable

Two-Years Clinical Performance of Bulk-Fill High Viscosity Ormocer Versus Methacrylate-Based Resin Composite Restorative Systems: The Effect of Bulk-Fill Low-viscosity Resin Composite Liners in Class II Restorations.

Mansoura University1 site in 1 country30 target enrollmentStarted: January 15, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
clinical performance

Study Overview

Brief Summary

This randomized clinical trial evaluated the clinical performance of class II resin composite restorations using bulk-fill high-viscosity ormocer versus methacrylate-based with or without a thin layer of bulk-fill low-viscosity (flowable) resin composite liners (BLRC) over 2 years. The null hypotheses in the study were as follows: (1) Different types of matrix structures (ormocer vs. methacrylate) have no effect on the marginal integrity of restorations; (2) A layer of bulk-fill resin compo-site liner of the same category would not affect the marginal or internal adaptation of restorations.

Detailed Description

The study was designed following the Consolidated Standards of Reporting Trials (CONSORT) statement. approvement by the local ethics committee of Mansoura University code register was taken code M 11120520. The patients were selected as they searched for treatment in the Conservative Dentistry Department outpatient clinic, in the Faculty of Dentistry, Mansoura University. A group of 30 patients 21 Females and 9 males was chosen from among 92 participants after careful consideration of the inclusion and exclusion criteria. The sample size estimate was made based on the clinical success rate of posterior class II composite restorations observed in a prior study (97.5% at 24 months). The sample size needed per group was 23 teeth using a significance level of 0.05, power of 80%, and equivalency limit of 15%. A total of 30 patients were chosen, for a total of 120 restorations (30 for each group) after taking potential dropouts into account. To ensure adherence of the participants to the study, all volunteers underwent complete dental treatment and periodic follow-ups. The volunteers were contacted by telephone, WhatsApp message, Facebook, and e-mail for the assessments. Four attempts, including visits to the schools, were made to contact a volunteer before he/she was considered a "loss." both participants and examiners were blind to the interventions. An inter-examiner and intra-examiner agreement of at least 90% was requested before the beginning of the evaluation. Clinical evaluation was performed one week after finishing and polishing (baseline), after 6 months, 12 months, 18 months, and 24 months using the World Dental Federation (FDI) criteria.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 33 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients having at least 4 posterior teeth with moderate occlusal-proximal carious lesions.
  • •Patients ranging in age from 18 to 30 years.
  • •patients with normal occlusion.

Exclusion Criteria

  • •General exclusion criteria:
  • •Patients having severe chronic periodontitis.
  • •Patients with orthodontic appliances.
  • •Abnormal occlusion, parafunctional habits.
  • •Allergy to any of the materials used in the study. Specific teeth exclusion criteria
  • •Teeth with irreversible pulpitis or non-vital.
  • •Fractured or cracked teeth.
  • •Previously restored teeth.
  • •Cavities with isthmus larger than intercuspal distance.
  • •Teeth with deep sub-gingival cavity margins.

Arms & Interventions

Xtra-fill

Active Comparator

Bulk-fill high-viscosity methacrylate-based resin composites.

Intervention: Xtra-fill (Combination Product)

X-base

Active Comparator

Bulk-fill low-viscosity methacrylate-based resin composites.

Intervention: x-base (Combination Product)

Admira fusion x-tra

Active Comparator

Bulk-fill high-viscosity ormocer-based resin composites.

Intervention: Admira fusion x-tra (Combination Product)

Admira fusion x-base

Active Comparator

Bulk-fill low-viscosity ormocer-based resin composites.

Intervention: Admira fusion x-base (Combination Product)

Outcomes

Primary Outcomes

clinical performance

Time Frame: two years

FDI criteria

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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