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NCT Number: NCT07029880

Clinical Performance of Metal Ceramic Fixed Dental Prostheses Using Two Porcelain Veneering Systems: A Randomized Clinical Trial

This study aims to evaluate the clinical performance of metal ceramic fixed dental prostheses veneered with two porcelain systems; Vintage Pro and IPS style ceram and cemented with Beautilink SA cement.

Recruiting

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cairo University

Cairo, Egypt

Location status: Recruiting

Location contact

Faculty of Dentistry Cairo University

CONTACT

00201008402645

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • Age ≥ 21 years
  • Vital or endodontically treated teeth
  • Abutments with no mobility
  • Abutments with adequate crown/root ratio more than 1:1
  • Willing and able to provide written informed consent
  • Ability to attend all follow-up appointments
  • Adequate oral hygiene as determined by the investigator

And the following exclusion criteria:

  • Patients with active periodontal disease (probing depth > 4mm, bleeding on probing)
  • Patients with parafunctional habits (e.g., bruxism confirmed by clinical examination)
  • Poor oral hygiene (plaque index > 30%)
  • Pregnancy or nursing
  • Systemic diseases affecting treatment outcomes (e.g., uncontrolled diabetes, immunosuppression)
  • Known allergies to study materials (alloy, ceramic, or resin cement components)
  • Inability to comply with study requirements
  • Current participation in other dental clinical trials
  • Active orthodontic treatment

Treatment and study plan

full veneered metal ceramic dental prosthesis cemented with resin cement

Other

full veneered metal ceramic dental prosthesis cemented with resin cement

Primary outcomes

  1. Wear

    Time frame: 18 months

    Measuring device :Digital software (Geomagic) .Measuring Unit :Root mean square

Secondary outcomes

  1. Restoration Failure

    Time frame: 18 months

    Measuring device: Modified USPHS criteria.Measuring Unit:Alpha: none Bravo: Discrete crack .Charlie: Chipping.Delta: Bulk fracture

  2. Luster of restoration

    Time frame: 18 months

    Measuring device:Modified USPHS criteria Measuring Unit :Alpha: restoration is shiny has enamel like translucent surface.Bravo: restoration is dull and somewhat opaque .Charlie: restoration surface is distinctly dull and opaque.

  3. Color match

    Time frame: 18 months

    Measuring device:Modified USPHS criteria. Measuring Unit:Alfa: no mismatch in color, shade and translucency between restoration and adjacent teeth Bravo: slight mismatch.Charlie: esthetically unacceptable mismatch

  4. Surface texture

    Time frame: 18 months

    Measuring device:Modified USPHS criteria.Measuring Unit:Alfa: Smooth, glazed or glossy surface.Bravo: Slightly rough surface.Charlie: Very rough surface

Study contacts

Contact information is provided by the study sponsor or research team.

inas adel mahmoud, lecturer

CONTACT

[email protected]

+201008402645

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2027
First posted
Jun 19, 2025
Registry last updated
Jun 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.