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Longevity of immediate esthetic rehabilitation with direct fiber reinforced composite fixed partial dentures

Longevity of immediate esthetic rehabilitation with direct fiber reinforced composite fixed partial dentures

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021293
Enrollment
100
Registered
2020-04-14
Start date
2020-04-20
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Z46.3

Interventions

Group 1: Preparation of the mock-up All bridges of this study were made with the stamp technique. As precondition for this technique a mock-up of the future pontic is made intraorally with composite o
Optibond FL Pimer and Adhesive, Kerr, Bioggio, Switzerland). In case of an adjacent porcelain or gold surface an adhesion protocol with Cojet (CoJet Sand
ESPE–particle size 30 µm, pressure 30 psi), silane (Monobond plus, Ivoclar, Schaan, Liechtenstein) and bonding agent was performed. The adhesive was light cured (Bluephase, IVoclar Vivaden, Schaan, Li

Sponsors

Universität BernKlinik für Zahnerhaltung, Präventiv- und Kinderzahnmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria are as followed: • adhesively bonded direct FRC-FPD including o anterior or posterior teeth o lower or upper jaws o one or two pontics o uni- or bilateral extensions o with and without a preparation in the abutment teeth

Exclusion criteria

Exclusion criteria: Exclusion criteria are as followed: • indirect FRC-FPD • no follow-up

Design outcomes

Primary

MeasureTime frame
Clinical assessment of the status of the DFRC-FPD will be done by the dentist who placed the restoration when patients attend for routine care, recall or when a problem occurrs. The observation period will start with the insertion of the DFRC-FPD. Primary Outcome (Functional survival): The intervention was considered as a ‘survival’ if the type of restoration was still the same. Consequently, repair or replacement of the DFRC-FPD was considered as survival. Whenever a different restoration type was inserted, an abutment tooth extracted or one of these treatments scheduled at the last check-up intervention was defined as failure (primary aim).

Secondary

MeasureTime frame
Secondary Outcome (Success): When the restoration was still in function at the last check-up visit and without any need of therapy, the intervention was defined as success. Whenever the restoration was replaced, repaired, recemented or scheduled for these treatments at the last check-up the intervention was defined as failure .

Countries

Switzerland

Contacts

Public ContactPhilippe Perrin

Universität BernKlinik für Zahnerhaltung, Präventiv- und Kinderzahnmedizin

philippe.perrin@zmk.unibe.ch+41 31 632 25 80

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026