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.
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
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 group | Role | What they receive |
|---|---|---|
| Veneered high-translucent zirconium dioxide fixed dental prosthesis | Experimental | Core 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 prosthesis | Active comparator | High 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.
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.
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)
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.
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.
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.
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.
- First posted8 Apr 2024
- Study start20 Dec 2017
- Primary completion27 Sep 2019
- Study completion20 Jan 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Missing TeethStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Malmö University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Emma Gardell, Principal investigator, Malmo university
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.
Study at a glance
From the registry record, last updated by the sponsor on 26 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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.
- ClinicalTrials.gov ID
- NCT06352983
- Acronym / sponsor ID
- 2014/11
- Conditions
- Missing Teeth
- Keywords
- dental ceramics, zirconium dioxide, randomized controlled trial, monolithic, FDP
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 31 participants (actual)
- Lead sponsor
- Malmö UniversityUniversity, hospital or other
- Study start
- 20 Dec 2017 (actual)
- Primary completion
- 27 Sep 2019 (actual)
- Study completion
- 20 Jan 2023 (actual)
- First posted
- 8 Apr 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| Veneered high-translucent zirconium dioxide fixed dental prosthesis | Experimental | Procedure: Fixed dental prosthesisCore material: high translucent zirconium dioxide (BruxZir, Glidewell, Newport Beach, Canada) Buccal veneer: porcelain (GC initial Zr, GC Corporation, Tokyo, Japan). |
| Monolithic high-translucent zirconium dioxide fixed dental prosthesis | Active comparator | Procedure: Fixed dental prosthesisHigh translucent zirconium dioxide (BruxZir, Glidewell, Newport Beach, Canada) |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Patients who needed an FDP replacing one or two missing teeth in the posterior dentition (premolars and/or molars).
Key exclusion criteria (1 listed)
- High caries activity Active periodontal disease Previously known history of repeated fractures of filings and/or reconstructions.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Fixed dental prosthesisFixed dentals prosthesis made out of high translucent zirconium dioxide with or without a porcelain veneer. | Procedure or surgery | Monolithic high-translucent zirconium dioxide fixed dental prosthesis, Veneered high-translucent zirconium dioxide fixed dental prosthesis |
Primary outcome
Fractures
Time frame: 4 years; From cementation of the fixed dental prosthesis up to the final evaluation.
Minor or major fractures of the fixed dental prosthesis material
De-bonding
Time frame: 4 years; From cementation of the fixed dental prosthesis up to the final evaluation.
Loss of retention of the fixed dental prosthesis.
4 secondary outcomes
Caries
Time frame: 4 years; From cementation of the fixed dental prosthesis to the final evaluation.
Endodontic
Time frame: 4 years; From cementation of the fixed dental prosthesis to the final evaluation.
Function
Time frame: 4 years; From cementation of the fixed dental prosthesis to the final evaluation.
Esthetics
Time frame: 4 years. From cementation of the fixed dental prosthesis to the final evaluation.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Nov 2025.
- Individual participant dataSharing planned: No. The study began enrolling patients before January 1 2019.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Emma Gardell principal investigator
Malmo university
2 sites in 1 country: see every site and its status.
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.