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The Clinical Performance of Inlay Zirconia Bridges

D

Damascus University

Status

Completed

Conditions

Dental Crowns

Treatments

Procedure: Glaze layer
Procedure: E-max Press layer

Study type

Interventional

Funder types

Other

Identifiers

NCT02995876
UDDS-FixPro-02-2016

Details and patient eligibility

About

When missing tooth structure or teeth are replaced, minimal biologic risk should be involved to re-establish function and esthetics. The increased use of the adhesive technique and preservation of dental tissues have greatly impacted conservative tooth preparation design. The development use of zirconia technology and all-ceramic systems has opened the potential for fabrication inlays zirconia bridges with durability and good aesthetics.

The purpose of this study is to clinically evaluate the placement of inlay bridge made of a Y-TZP framework veneered with a pressed ceramic and bonded with a completely adhesive approach in the replacement of a single missing tooth.

Full description

This study evaluates the use of inlay bridge made of Zirconia and all ceramic systems with three designs in the replacement process of one single tooth (i.e. a missing premolar or molar.) The first design is going to be fabricated with CAD/CAM Zirconia and the occlusal surface from e-max press.

The second design is going to be fabricated with CAD/CAM Zirconia and the occlusal surface from e-max press and the internal surface coated with glaze layer to improve the adhesion.

The third design is going to be fabricated with CAD/CAM Zirconia and the occlusal surface from e-max press and the internal surface coated with a layer of e-max ceramic press to improve the adhesion.

Enrollment

30 patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Good oral hygiene
  2. Low susceptibility to caries
  3. Parallel alignment of abutment teeth
  4. Immobility of the abutment teeth
  5. Minimum height of abutment teeth ≥ 5 mm (connector thickness)
  6. Maximum mesio-distal extension of the inter-dental gap of 9 mm (width of premolar) or 12 mm (width of molar)

Exclusion criteria

  • Severe para-functional habits.
  • Short clinical crowns (<5 mm)
  • Extensive defects of the clinical crown,
  • Loosening of teeth because of factors related to the periodontal tissues.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 3 patient groups

Zirconia and E-max Press
No Intervention group
Description:
The first design is going to be fabricated with CAD/CAM Zirconia and the occlusal surface from E-max Press.
Zirconia and E-max Press and Glaze
Experimental group
Description:
The second design is going to be fabricated with CAD/CAM Zirconia and the occlusal surface from E-max Press and the internal surface coated with a glaze layer to improve adhesion.
Treatment:
Procedure: Glaze layer
Zirconia and E-max Press twice
Experimental group
Description:
The third design is going to be fabricated with CAD/CAM Zirconia and the occlusal surface from E-max Press and the internal surface coated with an E-max Press layer to improve adhesion.
Treatment:
Procedure: E-max Press layer

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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