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Clinical Evaluation of Dental Restorations in Composite Resin made 14 years ago

Clinical Evaluation of Restorations in Composite Resin Packable and micro-hybrids performed 14 years ago

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-8gcd45
Enrollment
Unknown
Registered
2018-02-07
Start date
2016-06-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Dental Restoration Wear

Interventions

A 14-year retrospective, analytical observational study in which a group of 07 patients underwent a clinical evaluation of their dental restorations on composite resins, evaluating the following: colo
Procedure/surgery
I01.409.418.750.600.650
SP1.011.122

Sponsors

Faculdade de Odontologia da Universidade Federal de Pernambuco
Lead Sponsor
Faculdade de Odontologia da Universidade Federal de Pernambuco
Collaborator

Eligibility

Age
No minimum to 65 Years

Inclusion criteria

Inclusion criteria: Patients with indication of restoration in at least 3 posterior teeth; good oral hygiene condition; healthy or properly restored antagonistic teeth.

Exclusion criteria

Exclusion criteria: Have made any changes in the restorations, replacements, repairs, prostheses; loss of dental elements analyzed in the study.

Design outcomes

Primary

MeasureTime frame
Expected Outcome 1: Satisfactory clinical performance of the restorations, after 14 years, verified using the USPHS (United State Public Healt Service) method, based on the observation of a variation of at least 5% in pre and post-intervention measurements, comparing 14-year clinical assessment compared to baseline.;Conclusion Found 1: It was observed that all the analyzed materials obtained a good clinical performance after 14 years. As for color reproducibility: score A (ideal) = 23.8%, B (acceptable) = 42.8%, C (unsatisfactory) = 28.57% and D (unsatisfactory) = 4.7%; discoloration of the superficial cavity margin: A score = 61.9%, B = 38.1%; caries recurrence: score A = 100%; wear and marginal integrity: score A = 9.5%, B = 80.9%, C = 9.5%.

Secondary

MeasureTime frame
Expected outcome 2: There would be statistically significant differences between the resins tested in the analyzed questions (color reproduction, marginal integrity, superficial cavo margin discoloration and loss of substance). From the observation of variation of the evaluations by at least 5%.;Conclusion 2: There were no statistically significant differences between the materials tested in this study (p> 0.281). - Color Playback: Filtek P60 (1 Alpha, 3 Bravo, 3 Charlie); Surefil (3 Alpha, 2 Bravo, 2 Charlie); Suprafill (1 Alpha, 4 Bravo, 1 Charlie, 1 Delta) = p = 0.958. - Discoloration of the Cavo Superficial Margin: Filtek P60 (3 Alpha, 4 Bravo); Surefil (5 Alpha, 2 Bravo; Suprafill (5 Alpha, 2 Bravo) = p = 0.281. - Presence of Caries: Filtek P60 (7 Alpha); Surefil (7 Alfa); Suprafill (7 Alfa) = p = 1.00. - Contour or Loss of Substance: Filtek P60 (6 Bravo, 1 Charlie); Surefil (7 Bravo); Suprafill (1 Alpha, 5 Bravo, 1 Charlie) = p = 0.746.

Countries

Brazil

Contacts

Public ContactLuis Espíndola

Faculdade de Odontologia da Universidade Federal de Pernambuco

lipe_espindola@hotmail.com+55(81)997867662

Outcome results

None listed

Source: REBEC (via WHO ICTRP)