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Clinical Evaluation of Posterior Indirect Resin Composite Restorations With PBE

NCT03832829 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2023-06-09

No results posted yet for this study

Summary

Evaluation of posterior indirect resin composite restorations with proximal box elevation technique.

Restoration of large posterior defects extending below the cemento-enamel junction (CEJ) with coverage of one or more cusps represent a very common clinical situation. When restoring deep cervical margins biological and technical operative problems may occur. In order to make clinical procedures less fault-prone 'Proximal Box Elevation' (PBE) is an option that refers to application of composite resin in the deepest parts of the proximal areas in order to reposition the cervical margin supragingivally prior to cavity preparation for an indirect restoration.

This project aims to evaluate the clinical performance and periodontal status of posterior indirect composite restorations with PBE. According to study design at least 60 patients will be recruited to project and 80 restorations will be evaluated. The project will be carried out at the School of Dentistry, Istanbul Medipol University,Turkey.

Conditions

  • Unsatisfactory or Defective Restoration of Tooth

Interventions

DEVICE

Indirect composite restoration

Restoration of tooth with extensive substance loss

Sponsors & Collaborators

  • Ivoclar Vivadent AG

    collaborator INDUSTRY

  • Istanbul Medipol University Hospital

    lead OTHER

Principal Investigators

  • Mutlu Özcan, DDS,PhD · University of Zurich

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-09-11
Primary Completion
2022-09-14
Completion
2025-09-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03832829 on ClinicalTrials.gov