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Missing TeethNCT06352983

Zirconium Dioxide Fixed Dental Prosthesis.

A study testing Fixed dental prosthesis in people with Missing Teeth, run by Malmö University at 2 sites in Sweden.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this clinical trial is to evaluate and compare bridges to replace one or two missing teeth in the mouth. The bridges will be made of two variants of ceramic material. We will evaluate the bridges for up to five years regarding technical and biological complications. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Missing Teeth
What is being tested?
Fixed dental prosthesis
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
31 participants
Where
2 sitesSweden
Study dates
20 Dec 2017to 20 Jan 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Patients who needed an FDP replacing one or two missing teeth in the posterior dentition (premolars and/or molars).

Who cannot join

  • High caries activity Active periodontal disease Previously known history of repeated fractures of filings and/or reconstructions.

Trial locations and contacts

2 sites in 1 country.

Sweden2 sites
  • Malmo university

    Malmö, Skåne County, 214 21

  • Malmo university

    Malmö, Skåne County, 21421

Other trials in Sweden

About this study

Official title: Monolithic- and Partially Veneered High-translucent Zirconium Dioxide (YSZ), a 4-year Follow-up of a Multicenter Prospective, Randomized Controlled Trial on Posterior FDPs.

The purpose of this clinical trial is to evaluate and compare bridges to replace one or two missing teeth in the mouth. The bridges will be made of two variants of ceramic material. We will evaluate the bridges for up to five years regarding technical and biological complications.

Read the detailed description

Purpose:

The purpose of this prospective randomized double blinded clinical trial is to systematically evaluate and compare the long-term durability of monolithic zirconium dioxide and veneered zirconium dioxide based 3-, 4- or 5-unit bridges in the posterior dentition over time. The durability will be evaluated by recording technical and biological complications.

Background:

Fixed dental prosthesis (FDP) therapy is a common therapy. Usually the FDPs are made by combining a metal frame with a veneer to give the body a more tooth-like appearance, known as porcelain-fused-to-metal.

For 20 years we have used ceramic frames as an alternative to metal, since it has better biological and aesthetic properties. A common complication with these newer materials, however, is that the porcelain veneer debonds from the substructure, which sometimes leads to a need for remaking the FDP.

Zirconium dioxide or yttria stabilized tetragonal polycrystalline zirconium dioxide (Y-TZP), is an oxide ceramic with excellent characteristics such as high strength and biocompatibility. We currently use this ceramic routinely in dentistry for the production of both crowns and FDPs. It is now a well-documented and reliable material.

The monolithic restorations, that is Y-TZP without veneer, have been developed over the past few years. The former core materials in Y-TZP were opaque white-colored but have recently undergone development to become much more esthetic by increased translucency and improving staining techniques, without losing strength. By using only the strong oxide ceramic throughout we can obtain strong materials that have good biological properties, but without the risk of porcelain veneering fractures.

Laboratory studies evaluating crown therapy have shown very good results regarding these monolithic materials, but clinical trials on FDPs are missing. The long-term clinical studies on FDPs available concern veneered Y-TZP which have achieved acceptable results with good survival rate but with some complications in the form of veneer fractures. The veneering technique and materials for Y-TZP FDPs have since been developed to decrease the risk of chip-off fractures and recent publications show promising results. The aim of this study is therefore to compare survival and complications rates of Y-TZP FDPs with veneer and without veneer, monolithic, respectively.

Question:

The null hypothesis for this study is that monolithic Y-TZP based FDPs will perform equivalent to the veneered Y-TZP based FDPs when used for constructions in the posterior dentition.

Study population:

Patients for the study will be recruited within the daily dental care operations at clinics in Public and Private Dental Services.

Study method and randomization:

Included patients will undergo treatment in the form of preparation of the teeth and an impression taken for FDP therapy. The dentist does not know which of the two different FDP materials his patient will receive. The dental laboratory will receive a requisition from the dentist with a code number. This code number is randomized to one of the two materials to be investigated. Half of the patients will get a veneered zirconia based FDP while the other half receives a monolithic zirconia based. The finished FDP will then be cemented in the same way regardless of material. Method of treatment, FDP materials and cementation is performed according to a standardized protocol used routinely in dentistry.

Evaluation methods:

The evaluation is done by recording technical and biological complications. The examination is conducted by intraoral inspection and photo documentation and is performed by dentists not involved in the performed treatments.

Quality control and reporting:

Will be published in a scientific journal.

Conditions
Missing Teeth
Being tested
Fixed dental prosthesis
Keywords
dental ceramics, zirconium dioxide, randomized controlled trial, monolithic, FDP
Medical subject headings
Anodontia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Fixed dental prosthesisProcedure or surgery

    Fixed dentals prosthesis made out of high translucent zirconium dioxide with or without a porcelain veneer.

Study groups in NCT06352983
Study groupRoleWhat they receive
Veneered high-translucent zirconium dioxide fixed dental prosthesisExperimentalCore material: high translucent zirconium dioxide (BruxZir, Glidewell, Newport Beach, Canada) Buccal veneer: porcelain (GC initial Zr, GC Corporation, Tokyo, Japan).
Receives: Procedure: Fixed dental prosthesis
Monolithic high-translucent zirconium dioxide fixed dental prosthesisActive comparatorHigh translucent zirconium dioxide (BruxZir, Glidewell, Newport Beach, Canada)
Receives: Procedure: Fixed dental prosthesis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Fractures

    Minor or major fractures of the fixed dental prosthesis material

    Measured: 4 years; From cementation of the fixed dental prosthesis up to the final evaluation.

  2. De-bonding

    Loss of retention of the fixed dental prosthesis.

    Measured: 4 years; From cementation of the fixed dental prosthesis up to the final evaluation.

Secondary outcomes (4)
  1. Caries

    Biological complication, presence of caries around the fixed dental prosthesis.

    Measured: 4 years; From cementation of the fixed dental prosthesis to the final evaluation.

  2. Endodontic

    Biological complication, if there had been a need of endodontic treatment during the evaluation period.

    Measured: 4 years; From cementation of the fixed dental prosthesis to the final evaluation.

  3. Function

    Patient-reported outcome, how the patient evaluate the function of the restoration. Modified interval scale.

    Measured: 4 years; From cementation of the fixed dental prosthesis to the final evaluation.

  4. Esthetics

    Patient-reported outcome, how the patient evaluate the esthetics of the restoration.Modified interval scale.

    Measured: 4 years. From cementation of the fixed dental prosthesis to the final evaluation.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Apr 2024
  2. Study start20 Dec 2017
  3. Primary completion27 Sep 2019
  4. Study completion20 Jan 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized controlled trial
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
31 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06352983
Sponsor's protocol ID
2014/11
Status last verified
Nov 2025
First submitted
20 Mar 2024
Last updated
26 Nov 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The study began enrolling patients before January 1 2019.

Questions about this trial

What is this clinical trial studying?

A study testing Fixed dental prosthesis in people with Missing Teeth, run by Malmö University at 2 sites in Sweden.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Fractures (time frame: 4 years; From cementation of the fixed dental prosthesis up to the final evaluation.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Nov 2025.

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