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Natural Dentition, Prosthesis and Antagonist Wear 3D Analysis

Natural Dentition, Prosthesis and Antagonist Wear 3D Analysis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05637619
Enrollment
36
Registered
2022-12-05
Start date
2022-01-01
Completion date
2024-12-31
Last updated
2024-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Prosthesis Complication, Wear, Occlusal, Wear, Tooth

Keywords

Tooth wear, Full arch Implant, 3D scanner, Prosthesis, Screw retained, Zirconia, Hybrid Acrylic

Brief summary

Wear resistance is one of the most important physical properties of teeth, and wear resistance of zirconia against artificial acrylic, enamel and composite resin denture teeth has not been clearly established. Implant-supported dental restorations present a higher threshold for occlusion perception when compared to natural teeth, which can occlusal overload mechanisms or lead to wear of rehabilitation materials or the antagonist arch. In clinical conditions, however, many other factors influence the complex interaction between dental enamel and opposing substrates: patient-related factors such as dietary habits, dysfunctional occlusion, masticatory forces, and bruxism contribute to accelerated enamel loss of antagonist teeth.

Detailed description

It will be our intention to perform a prospective study and proof-of-concept to assess wear in natural dentition, Full arch implant supported rehabilitation (FAISR) and opposing arches. Wear according to type of rehabilitation and of opposing arch, technical complications, parafunction and number of placed implants will be assessed. Intra-oral digital acquisition will be performed at pre-defined intervals. Changes over time will be assessed through a previously described digital superimposition methodology volumetric changes determined. Patients will be scanned using an intraoral dental scanner (T0) Patients will be recalled at every 4-months (T1), 8-months (T2) and 12-months (T3) visits for re-scanning and from there every 6-months Scanned images will be compared using a metrology software to determine maximum vertical wear of teeth and root mean square wear.

Interventions

Maxillary or/and mandibular screw retained zirconia monolithic prostheses supported by at least 4 implants

DEVICEHybrid-Acrylic

Maxillary or/and mandibular screw retained hybrid prostheses supported by at least 4 implants;

BEHAVIORALDentate Patients

Dentate Patients with natural dentition or tooth supported crowns

Sponsors

Implantology Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

Dentate Group : Inclusion criteria * fully dentate (with at least 10 teeth ) and do not have any tooth mobility; * at least 12months follow up

Exclusion criteria

\- missing more than 4 teeth, extensive caries, bonded orthodontic brackets Edentulous Group: Inclusion Criteria: * Maxilla or Mandible Implant full-mouth implant restoration * Monolithic ceramic or hybrid-acrylic restoration * at least12 months Follow-up

Design outcomes

Primary

MeasureTime frameDescription
Wear of teeth and materials of restorationsat least 12 months follow-upMeasure in different groups occlusal tooth wear from insertion (baseline) to 4, 8 and 12 months post-insertion Scanned images will be compared using a metrology software to determine maximum vertical wear of teeth and root mean square wear.

Secondary

MeasureTime frameDescription
Wear of different antagonistsat least 12 months follow-upMeasure occlusal tooth wear of antagonists from insertion (baseline) to 4, 8 and 12 months post-insertion Scanned images will be compared using a metrology software to determine maximum vertical wear of teeth and root mean square wear.

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026