Clinical Performance of Three Different Restorative Materials

ConditionTooth Disease
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorHacettepe University

About this trial

The clinical performance of a bioactive composite (alkasite-based), a nanohybrid resin composite and a bulk-fill resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 3 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into three groups: a bioactive composite \[Cention Forte Ivoclar Vivadent, Schaan, Liechtenstein\], a nanohybrid resin composite \[Tetric N-Ceram2 (Ivoclar Vivadent, Schaan, Liechtenstein)\] and a bulk-fill resin composite \[Tetric N-PowerFill2 (Ivoclar Vivadent, Schaan, Liechtenstein)\], All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

age range will be 18 to 65

patients should have at least 3 approximal caries lesions require restoration

healthy periodontal status

a good likelihood of recall availability

Disqualifiers

poor gingival health

adverse medical history

potential behavioral problems

Trial design

Design model

Parallel

Treatments tested in this trial

  • bioactive composite

    Device

    bioactive composite restoration

  • nanohybrid resin composite

    Device

    nanohybrid resin composite restoration

  • bulk-fill resin composite

    Device

    bulk-fill resin composite restoration

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: bioactive compositeExperimental treatment 1 intervention
Group B: nanohybrid resin compositeExperimental treatment 1 intervention
Group C: bulk-fill resin compositeExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Clinical performances of different restorative systems according to FDI criteria

Two year results according to FDI criteria (scores 1-5, 1-very good, 5-poor/replace)

Time frame
two years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: