Comparison of Clinical Performance of Partial Restorations Fabricated With Three-Dimensional Printer and CAD-CAM

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorCukurova University

About this trial

The aim of this clinical study is to compare CAD-CAM and 3D restorations in individuals with two hard tissue losses or restorations in their mouths. The main question it aims to answer is: Is there a difference between CAD-CAM and 3D restorations according to FDI criteria? Researchers will compare participants to see if there is a difference between the two restorations according to FDI criteria. In this split-mouth study, participants will be randomized to receive a CAD-CAM partial restoration on one tooth and a 3D partial restoration on the other tooth.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

Patients with excessive bruxism or parafunctional habits.

Pregnant or lactating women.

Patients with gum disease or severe bone loss.

Patients with a history of allergic reactions.

Trial design

Design model

Parallel

Treatments tested in this trial

  • 3D printer partial crown

    Other intervention

    Comprasion of partial restorations made with 3D printer

  • Treatment as usual

    Other intervention

    Cad-cam printer partial crown

Treatment groups

12 Participants
are divided into 2 treatment groups
Group A: 3D printer partial crownExperimental treatment 1 intervention
Group B: Cad-Cam partial crownOther 1 intervention

Trial outcomes

Primary outcomes

1

Clinical performance of dental restorations evaluated using FDI World Dental Federation criteria

Esthetic Properties Color match (shade stability) Surface staining Translucency/opacity Anatomical form preservation Functional Properties Fracture and retention Marginal adaptation (gap formation) Wear resistance Occlusal contact stability Biological Properties (Newly added) Postoperative hypersensitivity (pulp reactions) Secondary caries development Periodontal response (gingival inflammation, bleeding on probing) Tooth integrity (adjacent tooth structure)

Time frame
Baseline, six months, 12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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