3D-printed resin versus zirconia for implant crowns and short bridges in the lower front jaw
Official title: 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
Run by Menoufia University · NCT07522671 · Data updated 2026-11-12
This trial tests whether 3D-printed permanent resin crowns and short fixed bridges work as well as milled zirconia for adults needing one or two implants in the lower front jaw.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Menoufia University Academic / other |
| Locations | 1 site (Shibīn al Kawm) |
| Status | Recruiting |
| Started | April 1, 2026 |
| Main results expected | April 1, 2027 |
| Study ends | November 1, 2028 |
| Registry record updated | April 13, 2026 |
| Trial ID | NCT07522671 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (≥18 years) who have one or two osseointegrated implants in the mandibular anterior region with stable peri-implant tissues, good oral hygiene, and need a single implant crown or a short (≤3-unit) implant-supported bridge are ideal candidates.
✕Probably not a fit
Patients with severe parafunctional habits (e.g., bruxism), uncontrolled systemic conditions affecting bone healing, peri-implantitis or unstable implants, or those needing long-span or non-mandibular-anterior prostheses are unlikely to benefit from this protocol.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a randomized, parallel-arm clinical trial comparing 3D-printed permanent resin (CROWNTEC) restorations to conventionally milled monolithic zirconia for implant-supported single crowns and short-span fixed partial dentures in the mandibular anterior region. All prostheses are produced using a standardized fully digital workflow (intraoral scanning, CAD design, and controlled fabrication) and delivered as screw- or cement-retained restorations. Participants are followed at baseline, 3, 6, and 12 months with planned extended follow-up, and the primary outcome is restoration survival over 12 months. Secondary outcomes include technical complications (fracture, chipping, screw loosening), peri-implant biological measures, marginal bone level changes on radiographs, and patient-reported satisfaction.
Why it matters
Potential benefit: If successful, this could offer a faster and potentially lower-cost alternative to zirconia with comparable short-term survival and patient satisfaction for implant restorations.
How similar studies have gone: Laboratory data and short-term clinical reports on 3D-printed resins show promising mechanical and esthetic results, but high-quality randomized clinical evidence for definitive 3D-printed implant restorations remains limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants must meet all of the following: * Age ≥18 years. * Have one or two osseointegrated dental implants requiring prosthetic restoration. * Demonstrate stable peri-implant tissues with no signs of inflammation or implant mobility. * Maintain good oral hygiene and controlled periodontal status. * Require either: * A single implant-supported crown, or * A short-span (maximum 3-unit) implant-supported fixed partial denture (FPD) supported by two implants in the mandibular anterior region. Exclusion Criteria: * Participants are excluded if they have any of the following: * Severe parafunctional habits (e.g., bruxism). * Uncontrolled systemic diseases affecting bone metabolism or healing. * Peri-implantitis or compromised implant stability. * Requirement for cantilever prostheses or long-span restorations, or FPDs in areas other than the mandibular anterior region.
Where it's running
-
Mohammed Elsawy
Shibīn al Kawm, Egypt Recruiting
Study contacts
- Study coordinator: Mohammed A. Elsawy, PhD
- Email: mohamed.elsawy@dent.menofia.edu.eg
- Phone: 00201061314522
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.