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Trial record 50 of 119 for:    ZIRCONIUM

Y-TZP and In-mouth Low Thermal Degradation: A Prospective Clinical Study

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ClinicalTrials.gov Identifier: NCT02150226
Recruitment Status : Active, not recruiting
First Posted : May 29, 2014
Last Update Posted : August 7, 2019
Sponsor:
Collaborator:
DMG Paris Descartes
Information provided by (Responsible Party):
Mainjot Amélie, University of Liege

Brief Summary:
The objective of this work is to study in-mouth aging and LTD of monolithic zirconia restorations. Microstructural changes characteristic of LTD processes, wear, and clinical behaviour following standard parameters will be evaluated. Notably Raman spectroscopy and 3D laser surface analysis will be used, directly on the restorations, which will be removed at regular intervals.The working hypothesis is that LTD process is very slow at the scale at the lifespan of dental prostheses.

Condition or disease Intervention/treatment Phase
Zirconia Monolithic Dental Restorations: In-mouth Behaviour, LTD and Wear Device: Lava plus (3M) crowns and bridges Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 101 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Low Thermal Degradation of Monolithic Zirconia Prostheses: an up to 5-year Original Prospective Clinical Study Using ex Vivo Analyses
Study Start Date : February 2014
Actual Primary Completion Date : April 2016
Estimated Study Completion Date : April 2021

Resource links provided by the National Library of Medicine

Drug Information available for: Zirconium

Arm Intervention/treatment
Experimental: Experimental: Zirconia monolithic crowns and bridges
Evaluation of Lava Plus zirconia dental crowns and bridges
Device: Lava plus (3M) crowns and bridges
Zirconia monolithic dental crowns and bridges evaluation




Primary Outcome Measures :
  1. in-mouth LTD of monolithic zirconia restorations on natural teeth and implants [ Time Frame: up to 5 years ]


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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Full zirconia crowns in the posterior region (molar/premolar)
  • On teeth or implants
  • Single unit restorations cemented on natural teeth and implants (including screw-retained restorations if possible, but no internal connections)
  • Multi-unit restorations on implants
  • If nightguard: to be performed on the antagonist

Exclusion Criteria:

  • Patients with removable prosthesis as an antagonist

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02150226


Locations
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Belgium
Institute of Dentistry University of Liege
Liege, Belgium, 4000
Sponsors and Collaborators
University of Liege
DMG Paris Descartes

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Mainjot Amélie, Doctor, University of Liege
ClinicalTrials.gov Identifier: NCT02150226     History of Changes
Other Study ID Numbers: FZ001
First Posted: May 29, 2014    Key Record Dates
Last Update Posted: August 7, 2019
Last Verified: August 2019