Minimal Invasive Rehabilitation of Tooth Loss in the Posterior Segment (MIZE-S)
MIZE-S
Clinical Performance of Two Different Designs of All-ceramic Resin-bonded Fixed Dental Prostheses in the Posterior Segment - a Randomized Controlled Pilot Study.
1 other identifier
interventional
30
1 country
1
Brief Summary
Tooth loss can be addressed by different rehabilitative strategies. Implant-supported crowns and conventional bridges (fixed dental prostheses \[FDPs\]) are well established treatment alternatives. Implant therapy is sometimes impossible, however, because of patient-related risk factors or economic issues. In such cases therapy with an FDP requires extensive removal of tooth structure to provide enough space for the restoration and to ensure mechanical retention if the abutment teeth are sound. Alternatives for rehabilitation requiring minor or no preparation of the anchoring teeth are desirable. Resin-bonded bridges meet this demand for minimal invasiveness and have been used clinically successfully. Sometimes, however, patients choose a conventional FDP over a resin-bonded one (RBFDP) for esthetic reasons since the adhesive wings, which are traditionally made of a cobalt-chromium alloy, might be exposed while speaking or smiling or account for a colour change of the abutment teeth. Such patients profit from an all-ceramic RBFDP. Today, the clinical performance of different all-ceramic RBFDP designs has not yet been evaluated under randomized controlled conditions. The aim of this pilot study is to calculate the sample size that allows us to accept the hypothesis that the two designs tested are similar regarding their clinical performance with adequate statistical power.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2013
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2013
CompletedFirst Submitted
Initial submission to the registry
November 18, 2013
CompletedFirst Posted
Study publicly available on registry
November 28, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedDecember 18, 2023
December 1, 2023
12.3 years
November 18, 2013
December 15, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Success
restoration/abutment teeth without intervention according to the Fédération dentaire internationale (FDI) World dental federation criteria
24 months
Secondary Outcomes (1)
restoration and antagonist wear
12 months, 24 months, 36 months
Study Arms (2)
all-ceramic inlay-retained RBFDP
EXPERIMENTALTreatment with an all-ceramic inlay-retained RBFDP
all-ceramic RBFDP
ACTIVE COMPARATORTreatment with an all-ceramic RBFDP
Interventions
Rehabilitation of tooth loss with an all-ceramic inlay-retained RBFDP
Eligibility Criteria
You may qualify if:
- missing second premolar, or first molar, or second molar
- regular patient of the department of prosthodontics of the university hospital of heidelberg
- willingness to return for recall examinations on a regular basis
- written informed consent
- abutment teeth are vital or sufficiently endodontically treated
- abutment teeth are periodontally stable
- abutment teeth have only little or no defects of the hardsubstances
You may not qualify if:
- Pregnancy or breastfeeding
- medically compromised condition not allowing for standard dental treatment
- Patient is not able to give written informed consent
- alcohol or drug abuse
- positive bruxism and parafunctions questionaire
- Bite-Strip \> 2
- Attrition Score \> 3
- deep bite (Angle class II/2)
- abutment tooth height \< 4mm
- missing canine or first premolar
- gap size \> 18 mm
- untreated symptomatic periodontal or endodontic lesions
- abutment tooth mobility \> grade I
- known allergies to materials used in this study
- poor dental hygiene
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Prosthodontics, University Hospital Heidelberg, University of Heidelberg
Heidelberg, Baden-Wurttemberg, 69120, Germany
Related Publications (2)
Bomicke W, Rathmann F, Pilz M, Bermejo JL, Waldecker M, Ohlmann B, Rammelsberg P, Zenthofer A. Clinical Performance of Posterior Inlay-Retained and Wing-Retained Monolithic Zirconia Resin-Bonded Fixed Partial Dentures: Stage One Results of a Randomized Controlled Trial. J Prosthodont. 2021 Jun;30(5):384-393. doi: 10.1111/jopr.13258. Epub 2020 Oct 4.
PMID: 32924240RESULTBomicke W, Rathmann F, Rammelsberg P, Zenthofer A. Three-year performance of inlay-retained or wing-retained zirconia resin-bonded fixed partial dentures - results from a randomized clinical pilot study. J Dent. 2025 Aug;159:105807. doi: 10.1016/j.jdent.2025.105807. Epub 2025 May 6.
PMID: 40339895DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Wolfgang Bömicke, Priv.-Doz. Dr. med. dent.
Department of Prosthodontics, University Hospital Heidelberg, University of Heidelberg
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr. med. dent.
Study Record Dates
First Submitted
November 18, 2013
First Posted
November 28, 2013
Study Start
October 1, 2013
Primary Completion
January 1, 2026
Study Completion
January 1, 2026
Last Updated
December 18, 2023
Record last verified: 2023-12