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Clinical Evaluation of Direct and Indirect Composites

Clinical Evaluation of Posterior Restorations Made With Direct and Indirect Composites

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06667271
Enrollment
90
Registered
2024-10-31
Start date
2023-03-16
Completion date
2025-11-01
Last updated
2026-01-07

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

Conditions

Dental Caries

Keywords

Dental caries, Restorative material, Composite resin, Indirect restorarion

Brief summary

The most commonly used materials in the treatment of decayed teeth are amalgam and composite resins. Because amalgam cannot meet the aesthetic expectations of patients and the rapidly increasing belief that it is toxic, its use has decreased considerably. Although composite resins are primarily used in anterior teeth because they provide aesthetically satisfactory results, they have also become the most preferred material in posterior teeth. This shift is largely due to the significant advancements in their mechanical properties, such as improved strength and durability. Indirect restorations have begun to be used to overcome the disadvantages of resin composites applied with the direct method. Both composite resins and ceramics have given good results for such restorations. However, composite resins have the advantage of being cheaper, more user-friendly, and repairable than ceramics. Laboratory-prepared composite inlays/onlays are more wear-resistant than direct composites, especially in occlusal contact areas. Therefore, they are generally indicated for the restoration of large cavities. Considering the material loss caused by crown restorations and the disadvantages of direct composites in the treatment of teeth with extensive caries, we aimed to treat indirect resin composites that we can apply by making more minimally invasive preparations while supporting the dental tissues.

Detailed description

This study was a double-blind randomized controlled clinical trial involving both evaluators and patients. The research compared indirect restorations with direct restorations. Patients receiving treatment were recalled for follow-ups after one week, six months, and twelve months. Restorations were assessed clinically based on modified FDI criteria, which included marginal discoloration, color match, anatomical form, fracture and retention, marginal adaptation, contact point, postoperative sensitivity, secondary caries, and periodontal response. Qualified clinicians conducted the evaluations using a mirror and probe under reflector light. Additionally, bite-wing radiographs were obtained from patients during the 6-month and 12-month follow-ups to assess the development of secondary caries. Differences between adhesives at each time point were analyzed using Fisher's Exact test, while the effect of time on restorations was evaluated with the Wilcoxon Signed Rank test (p \< 0.05).

Interventions

None listed

Sponsors

Recep Tayyip Erdogan University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* They have been informed about the study and have agreed to participate. * They are over 18 years old. * They do not have any systemic diseases. * They maintain good general oral health. * They are not pregnant or breastfeeding. * The relevant tooth is vital, and the decay is at least 0.5 mm away from the pulp, as confirmed by radiographic findings. * There is a tooth in contact with the relevant tooth and an antagonist tooth. * They have agreed to attend follow-up appointments.

Exclusion criteria

* After being informed about the study, the participant declined to participate. * The individual is under 18 years of age. * The volunteer has a severe systemic disease. * They have active periodontal or pulp disease. * They have received endodontic treatment. * They experience bruxism.

Design outcomes

Primary

MeasureTime frameDescription
World Dental Federation criteria (FDI)1 year1, Clinically very good; 2, clinically good; 3, clinically sufficient; 4, clinically unsatisfactory; 5, clinically poor

Countries

Turkey (Türkiye)

Outcome results

None listed

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