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

Comparison of Clinical Performance of Partial Restorations Fabricated With Three-Dimensional Printer and CAD-CAM: A Split-Mouth Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07031856
Enrollment
12
Registered
2025-06-22
Start date
2025-07-01
Completion date
2026-11-01
Last updated
2026-04-02

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

Conditions

Dental Caries, Dental Restoration, Permanent, Tooth Diseases

Brief summary

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.

Interventions

OTHER3D printer partial crown

Comprasion of partial restorations made with 3D printer

OTHERTreatment as usual

Cad-cam printer partial crown

Sponsors

Cukurova University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

İncluiding: \-- Patients with periodontally stable and appropriate oral hygiene habits without serious systemic diseases that preclude restoration. - Male and female patients with hard tissue loss in their mouth or with 2 teeth in need of restoration replacement (eligibility for split-mouth design). - People who can comply with the treatment and volunteer for follow-up for 2 years-

Exclusion criteria

Patients with systemic conditions that may affect the study process (e.g. diabetes, autoimmune diseases). * 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.

Design outcomes

Primary

MeasureTime frameDescription
Clinical performance of dental restorations evaluated using FDI World Dental Federation criteriaBaseline, six months, 12 monthsEsthetic 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)

Countries

Turkey (Türkiye)

Contacts

CONTACTResearch Assistant
yarenncoskun@gmail.com+90 0544 745 8633

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026