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Three-Year Clinical Performance of Fiber-reinforced Versus Indirect Resin Composite Posterior Restorations

Three-Year Clinical Performance of Fiber-reinforced Versus Indirect Resin Composite Posterior Restorations

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06803537
Enrollment
33
Registered
2025-01-31
Start date
2022-01-01
Completion date
2025-07-31
Last updated
2025-05-11

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

Conditions

Occlusal Caries, Proximal Caries

Keywords

fiber-reinforced composite, indirect lab composite, posterior restorations

Brief summary

This study aimed to perform a comparison between the clinical performance of short fiber-reinforced composite and indirect lab composite restorations in posterior dentition.

Interventions

OTHERFiber-reinforced composite

short fiber-reinforced composite used as base covered by conventional composite

OTHERindirect lab composite

indirect lab processed resin composite inlay restorations

conventional microhybrid resin composite posterior restorations

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. Patients aged 20-35 year from both genders. 2. Good oral hygiene: patients with low and moderate caries risk (according to Caries management by caries risk assessment CAMBRA sheets) were enrolled in this study. 3. The visual examination should reveal the presence of a minimum of three primary occlusal or proximal caries (Black Class I and II) with a severity score of 4 or 5 according to the International Caries Detection and Assessment System (ICDAS). 4. The carious teeth must exhibit vitality and do not display periapical radiolucency as evaluated by periapical radiography. 5. The selected teeth must be under stable occlusion.

Exclusion criteria

1. Uncontrolled systemic disease 2. Extremely poor oral hygiene 3. Chronic periodontitis 4. Heavy bruxism 5. Cavities with a buccolingual width exceeding two-thirds of the intercuspal distance or requiring cusp covering. 6. Patients undergoing orthodontic procedures. 7. Patients unable to attend the scheduled recall appointments.

Design outcomes

Primary

MeasureTime frame
FDI criteria for evaluationThree years follow-up

Countries

Egypt

Outcome results

None listed

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