Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
ID07522671

Clinical Performance of 3D-Printed Resin Versus Milled Monolithic Zirconia in Implant-Supported Single Crowns and Short-Span Fixed Partial Dentures: A Randomized Controlled Clinical Trial

Led by Menoufia University · Updated on 2026-04-13

60

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the clinical performance of implant-supported restorations made from 3D-printed permanent resin (CROWNTEC) compared with conventionally milled monolithic zirconia. The study focuses on single crowns and short-span fixed partial dentures in the front lower jaw, where function and appearance are important. This randomized controlled clinical trial aims to provide evidence on whether 3D-printed resin materials are a viable alternative to zirconia in implant prosthodontics. Participants are randomly assigned to two groups: one receiving restorations made with 3D-printed resin using a fully digital workflow including intraoral scanning, CAD design, 3D printing, post-processing, finishing, and polishing; the other group receives zirconia restorations made by CAD-CAM milling followed by sintering, finishing, and polishing. Both types of restorations are delivered as screw-retained or cement-retained prostheses. The study includes follow-up visits at baseline, 3, 6, and 12 months, with extended follow-up planned up to 24 months. During the study, participants will have assessments of restoration survival, technical complications like fracture or screw loosening, biological parameters including plaque index and probing depth, and radiographic evaluations of bone level changes. Patient satisfaction with esthetics, comfort, and chewing function is measured using questionnaires. The main outcome is the survival rate of restorations after 12 months. The study period extends up to two years, with ongoing monitoring to understand the performance and limitations of both materials.

CONDITIONS

Brief Title

Clinical Performance of 3D-Printed Resin and Zirconia Implant Restorations

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Have one or two dental implants that need prosthetic restoration
  • Stable tissues around the implant with no inflammation or implant mobility
  • Good oral hygiene and controlled gum health
  • Need either a single implant-supported crown or a short-span fixed partial denture (maximum 3 units) supported by two implants in the lower front jaw
Not Eligible

You will not qualify if you...

  • Severe teeth grinding or clenching habits (bruxism)
  • Uncontrolled systemic diseases affecting bone metabolism or healing
  • Peri-implantitis or unstable implants
  • Need for cantilever prostheses or long-span restorations
  • Fixed partial dentures in areas other than the lower front jaw

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Up to 1 month

Participants receive implant-supported single crowns or short-span fixed partial dentures fabricated using either 3D-printed permanent resin or milled monolithic zirconia through a fully digital workflow including intraoral scanning, CAD design, and standardized manufacturing protocols. Restorations are delivered as screw- or cement-retained prostheses.

1 baseline visit for prosthesis delivery

Post-operative Follow-up

Duration - 12 months with extended follow-up up to 24 months

Participants are followed to monitor restoration survival, technical complications, biological parameters, radiographic changes, and patient satisfaction over time.

Visits at 3, 6, and 12 months with possible extended visits up to 24 months

Trial Site Locations

Total: 1 location

1

Mohammed Elsawy

Shibīn al Kawm, Egypt, 2266166

Actively Recruiting

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Research Team

M

Mohammed A. Elsawy, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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